Integrin receptor antagonists

ABSTRACT

This invention relates to novel heterocycle compounds including but not limited to 3- 3- 3-(imidazolin-2-yl amino)propyloxy!isoxazol-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid, which are useful as antagonists of the α v  β 3  and related integrin receptors, to pharmaceutical compositions containing such compounds, processes for preparing such compounds, and to methods of using these compounds, alone or in combination with other therapeutic agents, for the inhibition of cell adhesion and the treatment of angiogenic disorders, inflammation, bone degradation, tumors, metastases, thrombosis, and other cell aggregation-related conditions.

FIELD OF THE INVENTION

This invention relates to novel heterocycles which are useful as antagonists of the α_(v) β₃ and related integrin receptors, to pharmaceutical compositions containing such compounds, processes for preparing such compounds, and to methods of using these compounds, alone or in combination with other therapeutic agents, for the inhibition of cell adhesion and the treatment of angiogenic disorders, inflammation, bone degradation, tumors, metastases, thrombosis, and other cell aggregation-related conditions.

BACKGROUND OF THE INVENTION

Angiogenesis or neovascularization is critical for normal physiological processes such as embryonic development and wound repair (Folkman and Shing, J. Biol. Chem. 1992, 267:10931-10934; D'Amore and Thompson, Ann. Rev. Physiol. 1987, 49:453-464). However, angiogenesis occurs pathologically, for example, in ocular neovascularization (leading to diabetic retinopathy, neovascular glaucoma, retinal vein occlusion and blindness), in rheumatoid arthitis and in solid tumors (Folkman and Shing, J. Biol. Chem., 1992, 267:10931-10934; Blood and Zetter, Biochim. Biophys. Acta., 1990, 1032:118-128).

Tumor dissemination, or metastasis, involves several distinct and complementary components, including the penetration and transversion of tumor cells through basement membranes and the establishment of self-sustaining tumor loci in diverse organ systems. To this end, the development and proliferation of new blood vessels, or angiogenesis, is critical to tumor survival. Without neovascularization, tumor cells lack the nourishment to divide and will not be able to leave the primary tumor site (Folkman and Shing, J. Biol. Chem., 1992, 267:10931-10934).

Inhibition of angiogenesis in animal models of cancer has been shown to result in tumor growth suppression and prevention of metastatic growth (Herblin et al., Exp. Opin. Ther. Patents. 1994, 1-14). Many angiogenic inhibitors have been directed toward blocking initial cytokine-dependent induction of new vessel growth, e.g. antibodies to endothelial cell growth factors. However, these approaches are problematic because tumor and inflammatory cells can secrete multiple activators of angiogenesis (Brooks et al., Cell, 1994, 79:1157-1164). Therefore, a more general approach that would allow inhibition of angiogenesis due to a variety of stimuli would be of benefit.

The integrin α_(v) β₃ is preferentially expressed on angiogenic blood vessels in chick and man (Brooks et al., Science, 1994, 264:569-571; Enenstein and Kramer, J. Invest. Dermatol., 1994, 103:381-386). Integrin α_(v) β₃ is the most promiscuous member of the integrin family, allowing endothelial cells to interact with a wide variety of extracellular matrix components (Hynes, Cell, 1992, 69:11-25). These adhesive interactions are considered to be critical for angiogenesis since vascular cells must ultimately be capable of invading virtually all tissues.

While integrin α_(v) β₃ promotes adhesive events important for angiogenesis, this receptor also transmits signals from the extracellular environment to the intracellular compartment (Leavesley et al., J. Cell Biol., 1993, 121:163-170, 1993). For example, the interaction between the α_(v) β₃ integrin and extracellular matrix components promotes a calcium signal required for cell motility.

During endothelium injury, the basement membrane zones of blood vessels express several adhesive proteins, including but not limited to von Willebrand factor, fibronectin, and fibrin. Additionally, several members of the integrin family of adhesion receptors are expressed on the surface of endothelial, smooth muscle and on other circulating cells. Among these integrins is α_(v) β₃, the endothelial cell, fibroblast, and smooth muscle cell receptor for adhesive proteins including von Willebrand factor, fibrinogen (fibrin), vitronectin, thrombospondin, and osteopontin. These integrins initiate a calcium-dependent signaling pathway that can lead to endothelial cell, smooth muscle cell migration and, therefore, may play a fundamental role in vascular cell biology.

Recently, an antibody to the α_(v) β₃ integrin has been developed that inhibits the interaction of this integrin with agonists such as vitronectin (Brooks et al., Science, 1994, 264:569-571). Application of this antibody has been shown to disrupt ongoing angiogenesis on the chick chorioallantoic membrane (CAM), leading to rapid regression of histologically distinct human tumor transplanted onto the CAM (Brooks et al., Cell, 1994, 79:1157-1164). In this model, antagonists of the α_(v) β₃ integrin induced apoptosis of the proliferating angiogenic vascular cells, leaving pre-existing quiescent blood vessels unaffected. Thus, α_(v) β₃ integrin antagonists have been shown to inhibit angiogenesis. Based on this property, therapeutic utility of such agents is expected in human diseases such as cancer, rheumatoid arthritis and ocular vasculopathies (Folkman and Shing, J. Biol. Chem., 1992, 267:10931-10934).

Increasing numbers of other cell surface receptors have been identified which bind to extracellular matrix ligands or other cell adhesion ligands thereby mediating cell-cell and cell-matrix adhesion processes. These receptors belong to a gene superfamily called integrins and are composed of heterodimeric transmembrane glycoproteins containing α- and β-subunits. Integrin subfamilies contain a common β-subunit combined with different α-subunits to form adhesion receptors with unique specificity. The genes for eight distinct β-subunits have been cloned and sequenced to date.

Two members of the β1 subfamily, α4/β1 and α5/β1 have been implicated in various inflammatory processes. Antibodies to α4 prevent adhesion of lymphocytes to synovial endothelial cells in vitro, a process which may be of importance in rheumatoid arthritis (VanDinther-Janssen et al., J. Immunol., 1991, 147:4207). Additional studies with monoclonal anti-α4 antibodies provide evidence that α4/β1 may additionally have a role in allergy, asthma, and autoimmune disorders (Walsh et al., J. Immunol., 1991, 146:3419; Bochner et al., J. Exp. Med., 1991 173:1553; Yednock et al., Nature, 1992, 356:63). Anti-α4 antibodies also block the migration of leukocytes to the site of inflammation (Issedutz et al., J. Immunol., 1991, 147:4178).

The α_(v) /β₃ heterodimer is a member of the β₃ integrin subfamily and has been described on platelets, endothelial cells, melanoma, smooth muscle cells, and osteoclasts (Horton and Davies, J. Bone Min. Res. 1989, 4:803-808; Davies et al., J. Cell. Biol. 1989, 109:1817-1826; Horton, Int. J. Exp. Pathol., 1990, 71:741-759). Like GPIIb/IIIa, the vitronectin receptor binds a variety of RGD-containing adhesive proteins such as vitronectin, fibronectin, VWF, fibrinogen, osteopontin, bone sialo protein II and thrombosponden in a manner mediated by the RGD sequence. A key event in bone resorption is the adhesion of osteoclasts to the matrix of bone. Studies with monoclonal antibodies have implicated the α_(v) /β₃ receptor in this process and suggest that a selective α_(v) /β₃ antagonist would have utility in blocking bone resorption (Horton et al., J. Bone Miner. Res., 1993, 8:239-247; Helfrich et al., J. Bone Miner. Res., 1992, 7:335-343).

European Patent Application Publication Number 525629 (corresponds to Canadian Patent Application Publication Number 2,074,685) discloses compounds having the general formula: ##STR1##

Copending, commonly assigned U.S. patent application Ser. No. 08/337,920 filed Nov. 10, 1994 discloses integrin inhibitors of the general formula shown below: ##STR2##

PCT Patent Application WO 94/08577 published Apr. 28, 1994 discloses fibrinogen antagonists, including the isoxazole-containing compound below: ##STR3##

None of the above references teaches or suggests the compounds of the present invention which are described in detail below.

SUMMARY OF THE INVENTION

The present invention provides novel nonpeptide compounds which bind to integrin receptors thereby altering cell-matrix and cell-cell adhesion processes. The compounds of the present invention are useful for the treatment of angiogenic disorders, inflammation, bone degradation, tumors, metastases, thrombosis, and other cell aggregation-related conditions in a meal.

One aspect of this invention provides novel compounds of Formula I (described below) which are useful as antagonists of the α_(v) /β₃ or vitronectin receptor. The compounds of the present invention inhibit the binding of vironectin to α_(v) /β₃ and inhibit cell adhesion. The present invention also includes pharmaceutical compositions containing such compounds of Formula I, and methods of using such compounds for the inhibition of angiogenesis, and/or for the treatment of angiogenic disorders.

The present invention also provides novel compounds, pharmaceutical compositions and methods which may be used in the treatment or prevention of diseases which involve cell adhesion processes, including, but not limited to, rheumatoid arthritis, asthma, allergies, adult respiratory distress syndrome, graft versus host disease, organ transplantation, septic shock, psoriasis, eczema, contact dermatitis, osteoporosis, osteoarthritis, atherosclerosis, metastasis, wound healing, diabetic retinopathy, ocular vasculopathies, thrombosis, inflammatory bowel disease and other autoimmune diseases.

Also included in the present invention are pharmaceutical kits comprising one or more containers containing pharmaceutical dosage units comprising a compound of Formula I, for the treatment of cell adhesion related disorders, including, but not limited to, angiogenic disorders.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides novel nonpeptide compounds of Formula I (described below) which bind to integrin receptors thereby altering cell-matrix and cell-cell adhesion processes. The compounds of the present invention are useful for the treatment of angiogenic disorders, inflammation, bone degradation, tumors, metastases, thrombosis, and other cell aggregation-related conditions in a mammal.

One aspect of this invention provides novel compounds of Formula I (described below) which are useful as antagonists of the α_(v) /β₃ or vitronectin receptor. The compounds of the present invention inhibit the binding of vitronectin to α_(v) /β₃ and inhibit cell adhesion. The present invention also includes pharmaceutical compositions containing such compounds of Formula I, and methods of using such compounds for the inhibition of angiogenesis, and/or for the treatment of angiogenic disorders.

1! The present invention comprises compounds of the Formula I: ##STR4## including stereoisomeric forms thereof, or mixtures of stereoisomeric forms thereof, or pharmaceutically acceptable salt or prodrug forms thereof wherein:

b, the bond between carbon atoms numbered 4 and 5, is a carbon-carbon single or double bond;

R¹ is selected from: ##STR5## A and B are independently --CH₂ --, --O--, --N(R¹²)--, or --C(═O)--;

A¹ and B¹ are independently --CH₂ -- or -N(R¹⁰)--;

D is --N(R^(2a))--, --O--, --S--, --C(═O)-- or --SO₂ --; E--F is --C(R²)═C(R³)--, --N═C(R²)--, --C(R²)═N--, --N═N--, or --C(R²)₂ C(R³)₂ --;

J, K, L and M are independently selected from --C(R²)-- or --N--, provided that at least one of J, K, L and M is --C(R²)--;

R² and R³ are independently selected from: H, C₁ -C₄ alkoxy, NR¹¹ R¹², ═NR¹², halogen, NO₂, CN, CF₃, C₁ -C₆ alkyl, C₃ -C₆ alkenyl, C₃ -C₇ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, C₆ -C₁₀ aryl, C₇ -C₁₁ arylalkyl, C₂ -C₇ alkylcarbonyl, C₆ -C₁₀ carbonyl or C₇ -C₁₁ arylcarbonyl;

alternatively, R² and R³, when substituents on adjacent atoms, can be taken together with the carbon atoms to which they are attached to form a 5-7 membered carbocyclic or 5-7 membered heterocyclic aromatic or nonaromatic ring system, said carbocyclic or heterocyclic ring being optionally substituted with 0-2 R⁷ ;

R^(2a) is absent or R¹² ;

U is selected from:

--(CH₂)_(n) --,

--(CH₂)_(n) O(CH₂)_(m) --,

--(CH₂)_(n) N(R¹²)(CH₂)_(m) --,

--(CH₂)_(n) C(═O)(CH₂)_(m) --,

--(CH₂)_(n) S(O)_(p) (CH₂)_(m) --,

--(CH₂)_(n) NHNH(CH₂)_(m) --,

--N(R¹⁰)C(═O)--, or

--C(═O)N(R¹⁰)--;

--N(R¹⁰)S(O)_(p) --, or

V is selected from:

--(CH₂)_(n) --,

--(C₁ -C₆ alkylene)-Q--, substituted with 0-3 groups independently selected from R¹³,

--(C₂ -C₇ alkenylene)-Q--, substituted with 0-3 groups independently selected from R¹³,

--(C₂ -C₇ alkynylene)-Q--, substituted with 0-3 groups independently selected from R¹³,

-(phenyl)-Q--, said phenyl substituted with 0-2 groups independently selected from R¹³,

-(pyridyl)-Q--, said pyridyl substituted with 0-2 groups independently selected from R¹³, or

-(pyridazinyl)-Q--, said pyridazinyl substituted with 0-2 groups independently selected from R¹³ ;

Q is selected from:

--(CH₂)_(n) --,

--(CH₂)_(n) O(CH₂)_(m) --,

--(CH₂)_(n) N(R¹²)(CH₂)_(m) --,

--(CH₂)_(n) C(═O)(CH₂)_(m) --,

--(CH₂)_(n) S(O)_(p) (CH₂)_(m) --,

--(CH₂)_(n) NHNH(CH₂)_(m) --,

--N(R¹⁰)C(═O)--, or

--C(═O)N(R¹⁰)--;

W is selected from:

--(C(R⁴)₂)_(q) C(═O)N(R¹⁰)--,

--C(═O)--N(R¹⁰)--(C(R⁴)₂)_(q) --;

X is selected from:

a single bond (i.e., X is absent),

--(C(R⁴)₂)_(q) -- C(R⁴)(R⁸)!_(s) --C(R⁴)(R⁹)--;

alternatively, W is ##STR6## and x is absent or --CH₂ --Y is selected from:

--COR²⁰, --SO₃ H, --PO₃ H, --CONHNHSO₂ CF₃, --CONHSO₂ R^(18a), --CONHSO₂ NHR^(18b), --NHCOCF₃, --NHCONHSO₂ R^(18a), --NHSO₂ R^(18a), --OPO₃ H₂, --OSO₃ H, --PO₃ H₂, --SO₃ H, --SO₂ NHCOR^(18a), --SO₂ NHCO₂ R^(18a), or ##STR7## Z is selected from --CH(R⁹)--, or --N(R¹⁶)--; R⁴ is selected from H, C₁ --C₁₀ alkyl, C₁ -C₁₀ alkylcarbonyl, aryl, arylalkyl, cycloalkyl, or cycloalkylalkyl;

alternatively, two R⁴ groups on adjacent carbon atoms may join to form a bond, thereby to form a carbon-carbon double or triple bond between the adjacent carbon atoms;

R⁵ is selected from H, C₁ -C₆ alkyl, C₂ -C₆ alkenyl, C₂ -C₆ alkynyl, C₃ -C₇ cycloalkyl, C₇ -C₁₄ bicycloalkyl, hydroxy, C₁ -C₆ alkoxy, C₁ -C₆ alkylthio, C₁ -C₆ alkylsulfinyl, C₁ -C₆ alkylsulfonyl, nitro, C₁ -C₆ alkylcarbonyl, C₆ -C₁₀ aryl, --N(R¹¹)R¹², halo, CF₃, CN, C₁ -C₆ alkoxycarbonyl, carboxy, piperidinyl, morpholinyl or pyridinyl;

R⁶ is selected from:

H, C₁ -C₁₀ alkyl, hydroxy, C₁ -C₁₀ alkoxy, nitro, C₁ -C₁₀ alkylcarbonyl, --N(R¹¹)R¹², cyano, halo, CF₃, CHO, CO₂ R^(18b), C(═O)R^(18b), CONR¹⁷ R^(18b), OC(═O)R¹⁰, OC(═O)OR²¹, OR¹⁰, OC(═O)NR¹⁰ R¹¹, OCH₂ CO₂ R¹⁰, CO₂ CH₂ CO₂ R¹⁰, NO₂, NR¹⁰ C(═O)R¹⁰, NR¹⁰ C(═O) OR²¹, NR¹⁰ C(═O)NR¹⁰ R¹¹, NR¹⁰ SO₂ NR¹⁰ R¹¹, NR¹⁰ SO₂ R²¹, S(O)_(p) R¹¹, SO₂ NR¹⁰ R¹¹, SiMe₃, C₂ to C₆ alkenyl, C₃ to C₁₁ cycloalkyl, C₄ to C₁₁ cycloalkylmethyl,

C₆ to C₁₀ aryl optionally substituted with 1-3 groups selected from halogen, C₁ -C₆ alkoxy, C₁ -C₆ alkyl, CF₃, S(O)_(m) Me, or --NMe₂ ;

C₇ to C₁₁ arylalkyl, said aryl being optionally substituted with 1-3 groups selected from halogen, C₁ -C₆ alkoxy, C₁ -C₆ alkyl, CF₃, S(O)_(p) Me, or --NMe₂,

methylenedioxy when R⁶ is a substituent on aryl, or a 5-10 membered heterocyclic ring containing 1-3 N, O, or S heteroatoms, wherein said heterocyclic ring may be saturated, partially saturated, or fully unsaturated, said heterocyclic ring being substituted with 0-2 R⁷ ;

R⁷ is selected from:

H, C₁ -C₁₀ alkyl, hydroxy, C₁ -C₁₀ alkoxy, nitro, C₁ -C₁₀ alkylcarbonyl, --N(R¹¹)R¹², cyano, halo, CF₃, CHO, CO₂ R¹⁰, C(═O)R¹⁰, CONR¹⁰ R¹¹, OC(═O)R¹⁰, OC(═O)OR²¹, OR¹⁰, OC(═O)NR¹⁰ R¹¹, OCH₂ CO₂ R¹⁰, CO₂ CH₂ CO₂ R¹⁰, NO₂, NR¹⁰ C(═O)R¹⁰, NR¹⁰ C(═O)OR²¹, NR¹⁰ C(═O)NR¹⁰ R¹¹, NR¹⁰ SO₂ NR¹⁰ R¹¹, NR¹⁰ SO₂ R²¹, S(O)_(p) R¹¹, SO₂ NR¹⁰ R¹¹, SiMe₃, C₂ to C₆ alkenyl, C₃ to C₁₁ cycloalkyl, C₄ to C₁₁ cycloalkylmethyl, C₆ to C₁₀ aryl, or C₇ to C₁₁ arylalkyl;

R⁸ is selected from:

H, R⁶,

C₁ -C₁₀ alkyl, substituted with 0-3 R⁶,

C₂ -C₁₀ alkenyl, substituted with 0-3 R⁶,

C₂ -C₁₀ alkynyl, substituted with 0-3 R⁶,

C₃ -C₈ cycloalkyl, substituted with 0-3 R⁶,

C₅ -C₆ cycloalkenyl, substituted with 0-3 R⁶,

aryl, substituted with 0-3 R⁶, or

5-10 membered heterocyclic ring containing 1-3 N, O, or S heteroatoms, wherein said heterocyclic ring may be saturated, partially saturated, or fully unsaturated, said heterocyclic ring being substituted with 0-2 R⁷ ;

R⁹ is selected from H, hydroxy, C₁ -C₁₀ alkoxy, nitro, N(R¹⁰)R¹¹, --N(R¹⁶)R¹⁷, OR²², C₁ -C₁₀ alkyl substituted with 0-3 R⁷, aryl substituted with 0-3 R⁷, heteroaryl substituted with 0-3 R⁷, C₁ -C₁₀ alkylcarbonyl; aryl(C₀ -C₆ alkyl)carbonyl, C₁ -C₁₀ alkenyl, C₁ -C₁₀ alkynyl, C₃ -C₁₀ cycloalkyl, C₃ -C₁₀ cycloalkylalkyl, aryl(C₁ -C₆ alkyl)-, heteroaryl(C₁ -C₆ alkyl)-, CO₂ R^(18a), C(═O)R^(18a), CONR^(18a) R²⁰, SO₂ R^(18a), or SO₂ NR^(18a) R²⁰, provided that any of the above alkyl, cycloalkyl, aryl or heteroaryl groups may be unsubstituted or substituted independently with 0-2 R⁷ ;

R¹⁰ is selected from H, C₁ -C₈ alkyl, C₃ -C₆ alkenyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylmethyl, C₆ -C₁₀ aryl, C₇ -C₁₁ arylalkyl, or C₁ -C₁₀ alkyl substituted with 0-2 R⁴ ;

R¹¹ is selected from hydrogen, hydroxy, C₁ to C₈ alkyl, C₃ -C₆ alkenyl, C₃ to C₁₁ cycloalkyl, C₄ to C₁₁ cycloalkylmethyl, C₁ -C₆ alkoxy, benzyloxy, C₆ to C₁₀ aryl, heteroaryl, heteroarylalkyl, C₇ to C₁₁ arylalkyl, adamantylmethyl, or C₁ -C₁₀ alkyl substituted with 0-2 R⁴ ;

alternatively, R¹⁰ and R¹¹ when both are substituents on the same nitrogen atom (as in --NR¹⁰ R¹¹) can be taken together with the nitrogen atom to which they are attached to form a heterocycle selected from:

3-azabicyclononyl, 1,2,3,4-tetrahydro-1-quinolinyl, 1,2,3,4-tetrahydro-2-isoquinolinyl, 1-piperidinyl, 1-morpholinyl, 1-pyrrolidinyl, thiamorpholinyl, thiazolidinyl or 1-piperazinyl; said heterocycle being optionally substituted with 0-3 groups selected from: C₁ -C₆ alkyl, C₆ -C₁₀ aryl, heteroaryl, C₇ -C₁₁ arylalkyl, C₁ -C₆ alkylcarbonyl, C₃ -C₇ cycloalkylcarbonyl, C₁ -C₆ alkoxycarbonyl, C₇ -C₁₁ arylalkoxycarbonyl, C₁ -C₆ alkylsulfonyl or C₆ -C₁₀ arylsulfonyl;

R¹² is selected from:

H, C₁ -C₁₀ alkyl, triphenylmethyl, methoxyphenyldiphenylmethyl, trimethylsilylethoxymethyoxy (SEM), C₁ -C₁₀ alkoxycarbonyl, C₁ -C₁₀ alkylcarbonyl, C₁ -C₁₀ alkylsulfonyl, aryl(C₁ -C₁₀ alkyl)sulfonyl, arylsulfonyl, aryl(C₂ -C₁₀ alkenyl)sulfonyl, heteroarylsulfonyl, aryl, C₂ -C₆ alkenyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, C₇ -C₁₁ arylalkyl, C₇ -C₁₁ arylcarbonyl, C₄ -C₁₁ cycloalkoxycarbonyl, C₇ -C₁₁ bicycloalkoxycarbonyl, C₇ -C₁₁ aryloxycarbonyl, heteroarylcarbonyl, heteroarylalkylcarbonyl, or aryl(C₁ -C₁₀ alkoxy)carbonyl; wherein said aryl groups are optionally substituted with 0-3 substituents selected from the group consisting of:

C₁ -C₄ alkyl, C₁ -C₄ alkoxy, halo, CF₃, and NO₂ ;

R¹³ is selected from: H, hydroxy, C₁ -C₁₀ alkoxy, nitro, N(R¹⁰)R¹¹, --N(R¹⁶)R¹⁷, C₁ -C₁₀ alkyl substituted with 0-3 R⁷, aryl substituted with 0-3 R⁷, heteroaryl substituted with 0-3 R⁷, or C₁ -C₁₀ alkylcarbonyl;

R¹⁴ is selected from H, C₁ -C₁₀ alkyl, C₂ -C₁₀ alkenyl, C₂ -C₁₀ alkynyl, C₁ -C₁₀ alkoxy, aryl, heteroaryl or C₁ -C₁₀ alkoxycarbonyl, CO₂ R¹⁰ or --C(═O)N(R¹⁰)R¹¹ ;

R¹⁵ is selected from:

H, R⁶, --CO₂ R¹⁰, --C(═O)N(R¹⁰)R¹¹ ;

C₁ -C₁₀ alkoxycarbonyl substituted with 0-2 R⁶ ;

C₁ -C₁₀ alkyl, substituted with 0-3 R⁶ ;

C₂ -C₁₀ alkenyl, substituted with 0-3 R⁶ ;

C₁ -C₁₀ alkoxy, substituted with 0-3 R⁶ ;

aryl, substituted with 0-3 R^(6;) or

5-10 membered heterocyclic ring containing 1-3 N, O, or S heteroatoms, wherein said heterocyclic ring may be saturated, partially saturated, or fully unsaturated, said heterocyclic ring being substituted with 0-2 R⁷ ;

R¹⁶ is selected from:

--C(═O)--O--R^(18a),

--C(═O)--R^(18a),

--C(═O)N(R^(18b))₂,

--C(═O)NHSO₂ R^(18a),

--C(═O)NHC(═O)R^(18b),

--C(═O)NHC(═O)OR^(18a),

--C(═O)NHSO₂ NHR^(18b),

--C(═S)--NH--R^(18b),

--NH--C(═O)--O--R^(18a),

--NH--C(═O)--R^(18b),

--NH--C(═O)--NH--R^(18b),

--SO₂ --O--R^(18a),

--SO₂ --R^(18a),

--SO₂ --N(R^(18b))₂,

--SO₂ --NHC(═O)OR^(18b) ;

R¹⁷ is selected from: H, C₁ -C₁₀ alkyl, C₂ -C₆ alkenyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₅ cycloalkylalkyl, aryl, aryl(C₁ -C₁₀ alkyl)-;

R^(18a) is selected from:

C₁ -C₈ alkyl substituted with 0-2 R¹⁹,

C₂ -C₈ alkenyl substituted with 0-2 R¹⁹,

C₂ -C₈ alkynyl substituted with 0-2 R¹⁹,

C₃ -C₈ cycloalkyl substituted with 0-2 R¹⁹,

aryl substituted with 0-4 R¹⁹,

aryl(C₁ -C₆ alkyl)- substituted with 0-4 R¹⁹,

a 5-10 membered heterocyclic ring system having 1-3 heteroatoms selected independently from O, S, and N, said heterocyclic ring being substituted with 0-4 R¹⁹,

C₁ -C₆ alkyl substituted with a 5-10 membered heterocyclic ring system having 1-3 heteroatoms selected independently from O, S, and N, said heterocyclic ring being substituted with 0-4 R¹⁹ ;

R^(18b) is selected from R^(18a) or H;

R¹⁹ is selected from H, halogen, CF₃, CO₂ H, CN, NO₂, NR¹¹ R¹², C₁ -C₈ alkyl, C₂ -C₆ alkenyl, C₂ -C₆ alkynyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, aryl(C₁ -C₆ alkyl)-, C₁ -C₆ alkoxy, OCF₃, or C₁ -C₄ alkoxycarbonyl, aryl, --O-aryl, --SO₂ -aryl, heteroaryl, or --SO₂ -heteroaryl, wherein said aryl and heteroaryl groups may be substituted with 0-4 groups selected from hydrogen, halogen, CF₃, C₁ -C₃ alkyl, or C₁ -C₃ alkoxy;

R²⁰ is selected from hydroxy, C₁ to C₁₀ alkyloxy, C₃ to C₁₁ cycloalkyloxy, C₆ to C₁₀ aryloxy, C₇ to C₁₁ arylalkyloxy, C₃ to C₁₀ alkylcarbonyloxyalkyloxy, C₃ to C₁₀ alkoxycarbonyloxyalkyloxy, C₂ to C₁₀ alkoxycarbonylalkyloxy, C₅ to C₁₀ cycloalkylcarbonyloxyalkyloxy, C₅ to C₁₀ cycloalkoxycarbonyloxyalkyloxy, C₅ to C₁₀ cycloalkoxycarbonylalkyloxy, C₇ to C₁₁ aryloxycarbonylalkyloxy, C₈ to C₁₂ aryloxycarbonyloxyalkyloxy, C₈ to C₁₂ arylcarbonyloxyalkyloxy, C₅ to C₁₀ alkoxyalkylcarbonyloxyalkyloxy, C₅ to C₁₀ (5-alkyl-1,3-dioxa-cyclopenten-2-one-yl)methyloxy, C₁₀ to C₁₄ (5-aryl-1,3-dioxa-cyclopenten-2-one-yl)methyloxy, (R¹¹)(R¹²)N--(C₁ -C₁₀ alkoxy)-;

R²¹ is selected from: C₁ -C₈ alkyl, C₂ -C₆ alkenyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylmethyl, C₆ -C₁₀ aryl, C₇ -C₁₁ arylalkyl, or C₁ -C₁₀ alkyl substituted with 0-2 R⁵ ;

R²² is selected from:

--C(═O)--R^(18b),

--C(═O)N(R^(18b))₂,

--C(═O)NHSO₂ R^(18a),

--C(═O)NHC(═O)R^(18b),

--C(═O)NHC(═O)OR^(18a),

--C(═O)NHSO₂ NHR^(18b),

--C(═S)--NH--R^(18b),

--SO₂ --R^(18a),

--SO₂ --N(R^(18b))₂,

--SO₂ --NHC(═O)OR^(18b) ;

m is 0-2;

n is 0-4;

p is 0-2;

q is 0-4;

r is 0-2;

s is 0-1;

with the following provisos:

(1) when b is a double bond, only one of R¹⁴ or R¹⁵ is present and Q and U are not --(CH₂)--; and

(2) n, m and q are chosen such that the number of atoms connecting R¹ and Y is in the range of 8-14; and

(3) when V is -(phenyl)-Q--, then either: U is not a direct bond (i.e., U is not --(CH₂)_(n) -- where n=0) or Q is not a direct bond (i.e., Q is not --(CH₂)_(n) -- where n=0).

2! Preferred compounds of the present invention are compounds of Formula I: ##STR8## including stereoisomeric forms thereof, or mixtures of stereoisomeric forms thereof, or pharmaceutically acceptable salt or prodrug forms thereof wherein:

b, the bond between carbon atoms numbered 4 and 5, is a carbon-carbon single or double bond;

R¹ is selected from: ##STR9## A is selected from --CH₂ --, or --N(R¹²)--; A¹ and B are independently --CH₂ -- or --N(R¹⁰)--;

D is --N(R¹²)--, or --S--;

E--F is --C(R²)═C(R³)--, or --C(R²)₂ C(R³)₂ --;

J is either --C(R²)-- or --N--, and K, L and M are independently selected from --C(R²)-- or --C(R³)--;

R² and R³ are independently selected from: H, C₁ -C₄ alkoxy, NR¹¹ R¹², ═NR¹², halogen, NO₂, CN, CF₃, C₁ -C₆ alkyl, C₃ -C₆ alkenyl, C₃ -C₇ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, C₆ -C₁₀ aryl substituted with 0-4 R⁷, C₇ -C₁₁ arylalkyl, C₂ -C₇ alkylcarbonyl, C₁ -C₄ alkoxycarbonyl, or C₇ -C₁₁ arylcarbonyl;

alternatively, R² and R³ when substituents on adjacent atoms, can be taken together when substituents on adjacent atoms, with the carbon atoms to which they are attached, to form a 5-7 membered carbocyclic or 5-7 membered heterocyclic with the carbon atoms to which they are attached, aromatic or nonaromatic ring system, said carbocyclic or heterocyclic ring being optionally substituted with 0-2 groups selected from C₁ -C₄ alkyl, C₁ -C₄ alkoxy, halo, cyano, amino, CF₃ or NO₂ ;

R^(2a) is absent or R¹² ;

U is selected from:

--(CH₂)_(n) --,

--(CH₂)_(n) O(CH₂)_(m) --,

--(CH₂)_(n) N(R¹²)(CH₂)_(m) --,

--(CH₂)_(n) C(═O)(CH₂)_(m) --,

--(CH₂)_(n) S(O)_(p) (CH₂)_(m) --,

--(CH₂)_(n) NHNH(CH₂)_(m) --,

--N(R¹⁰)C(═O)--, or

--C(═O)N(R¹⁰)--;

--N(R¹⁰)S(O)_(p) --, or

V is selected from:

--(CH₂)_(n) --,

--(C₁ -C₆ alkylene)-Q--, substituted with 0-3 groups independently selected from R¹³,

--(C₂ -C₇ alkenylene)-Q--, substituted with 0-3 groups independently selected from R¹³,

--(C₂ -C₇ alkynylene)-Q--, substituted with 0-3 groups independently selected from R¹³,

-(phenyl)-Q--, said phenyl substituted with 0-2 groups independently selected from R¹³,

-(pyridyl)-Q--, said pyridyl substituted with 0-2 groups independently selected from R¹³, or

-(pyridazinyl)-Q--, said pyridazinyl substituted with 0-2 groups independently selected from R¹³ ;

Q is selected from:

--(CH₂)_(n) --,

--(CH₂)_(n) O(CH₂)_(m) --,

--(CH₂)_(n) N(R¹²)(CH₂)_(m) --,

--(CH₂)_(n) C(═O)(CH₂)_(m) --,

--(CH₂)_(n) S(O)_(p) (CH₂)_(m) --,

--(CH₂)_(n) NHNH(CH₂)_(m) --,

--N(R¹⁰)C(═O)--, or

--C(=O)N(R¹⁰)--;

W is selected from:

--(C(R⁴)₂)_(q) C(═O)N(R¹⁰)-- or,

--C(═O)--N(R¹⁰)--(C(R⁴)₂)_(q) --;

X is selected from:

a single bond (i.e., X is absent) or,

--(C(R⁴)₂)_(q) -- C(R⁴)(R⁸)!_(s) --C(R⁴)(R⁹)--;

alternatively, W is ##STR10## and X is either absent or --CH₂ --Y is selected from:

--COR²⁰, --SO₃ H, --PO₃ H, --CONHNHSO₂ CF₃,

--CONHSO₂ R^(18a), --CONHSO₂ NHR^(18b), --NHCOCF₃,

--NHCONHSO₂ R^(18a), --NHSO₂ R^(18a), --OPO₃ H₂, --OSO₃ H,

--PO₃ H₂, --SO₃ H, --SO₂ NHCOR^(18a), --SO₂ NHCO₂ R^(18a), or ##STR11## Z is selected from --CH(R⁹)--, or --N(R¹⁶)--; R⁴ is selected from H, C₁ -C₁₀ alkyl, C₁ -C₁₀ alkylcarbonyl, aryl, arylalkyl, cycloalkyl, or cycloalkylalkyl;

alternatively, two R⁴ groups on adjacent carbon atoms may join to form a bond, thereby to form a carbon-carbon double or triple bond between the adjacent carbon atoms;

R⁶ is selected from:

H, C₁ -C₁₀ alkyl, hydroxy, C₁ --C₁₀ alkoxy, nitro, C₁ -C₁₀ alkylcarbonyl, --N(R¹¹)R¹², cyano, halo, CF₃, CHO, CO₂ R^(18b), C(═O)R^(18b), CONR¹⁷ R^(18b), OC(═O)R¹⁰, OR¹⁰, OC(═O)NR¹⁰ R¹¹, NR¹⁰ C(═O)R¹⁰, NR¹⁰ C(═O)OR²¹, NR¹⁰ C(═O)NR¹⁰ R¹¹, NR¹⁰ SO₂ NR¹⁰ R¹¹, NR¹⁰ SO₂ R²¹, S(O)_(p) R¹¹, SO₂ NR¹⁰ R¹¹,

C₆ to C₁₀ aryl optionally substituted with 0-3 groups selected from halogen, C₁ -C₆ alkoxy, C₁ -C₆ alkyl, CF₃, S(O)_(m) Me, or --NMe₂ ;

C₇ to C₁₁ arylalkyl, said aryl being optionally substituted with 1-3 groups selected from halogen, C₁ -C₆ alkoxy, C₁ -C₆ alkyl, CF₃, S(O)_(p) Me, or --NMe₂,

a 5-10 membered heterocyclic ring containing 1-3 N, O, or S heteroatoms, wherein said heterocyclic ring may be saturated, partially saturated, or fully unsaturated, said heterocyclic ring being substituted with 0-2 R⁷ ;

R⁷ is selected from selected from H, C₁ -C₄ alkyl, hydroxy, C₁ -C₄ alkoxy, C₆ -C₁₀ aryl, C₇ -C₁₁ arylalkyl, (C₁ -C₄ alkyl)carbonyl, CO₂ R^(18a), SO₂ R¹¹, SO₂ NR¹⁰ R¹¹, OR¹⁰, or N(R¹¹)R¹² ;

R⁸ is selected from:

H, CO₂ R^(18a), C(═O)R^(18a), or CONR¹⁷ R^(18a)

C₁ -C₁₀ alkyl, substituted with 0-1 R⁶,

C₂ -C₁₀ alkenyl, substituted with 0-1 R⁶,

C₂ -C₁₀ alkynyl, substituted with 0-1 R⁶,

C₃ -C₈ cycloalkyl, substituted with 0-1 R⁶,

C₅ -C₆ cycloalkenyl, substituted with 0-1 R⁶,

aryl, substituted with 0-3 R⁶, or

5-10 membered heterocyclic ring containing 1-3 N, O, or S heteroatoms, wherein said heterocyclic ring may be saturated, partially saturated, or fully unsaturated, said heterocyclic ring being substituted with 0-2 R⁷ ;

R⁹ is selected from H, hydroxy, C₁ -C₁₀ alkoxy, nitro, N(R¹⁰)R¹¹, --N(R¹⁶)^(R) ¹⁷, OR²², C₁ -C₁₀ alkyl substituted with 0-3 R⁷, aryl substituted with 0-3 R⁷, heteroaryl substituted with 0-3 R⁷, C₁ -C₁₀ alkylcarbonyl; aryl (C₀ -C₆ alkyl)carbonyl, C₁ -C₁₀ alkenyl, C₁ -C₁₀ alkynyl, C₃ -C₁₀ cycloalkyl, C₃ -C₁₀ cycloalkylalkyl, aryl (C₁ -C₆ alkyl)-, heteroaryl(C₁ -C₆ alkyl)-, CO₂ R^(18a), C(═O)R^(18a), CONR^(18a) R²⁰, SO₂ R^(18a), or SO₂ NR^(28a) R²⁰, provided that any of the above alkyl, cycloalkyl, aryl or heteroaryl groups may be unsubstituted or substituted independently with 0-2 R⁷ ;

R¹⁰ is selected from H, C₁ -C₈ alkyl, C₃ -C₆ alkenyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylmethyl, C₆ -C₁₀ aryl, C₇ -C₁₁ arylalkyl, or C₁ -C₁₀ alkyl substituted with 0-2 R⁴ ;

R¹¹ is selected from hydrogen, hydroxy, C₁ to C₈ alkyl, C₃ -C₆ alkenyl, C₃ to C₁₁ cycloalkyl, C₄ to C₁₁ cycloalkylmethyl, C₁ -C₆ alkoxy, benzyloxy, C₆ to C₁₀ aryl, heteroaryl, heteroarylalkyl, C₇ to C₁₁ arylalkyl, adamantylmethyl, or C₁ -C₁₀ alkyl substituted with 0-2 R⁴ ;

alternatively, R¹⁰ and R¹¹ when both are substituents on the same nitrogen atom (as in --NR¹⁰ R¹¹) can be taken together with the nitrogen atom to which they are attached to form a heterocycle selected from:

3-azabicyclononyl, 1,2,3,4-tetrahydro-1-quinolinyl, 1,2,3,4-tetrahydro-2-isoquinolinyl, 1-piperidinyl, 1-morpholinyl, 1-pyrrolidinyl, thiamorpholinyl, thiazolidinyl or 1-piperazinyl; said heterocycle being optionally substituted with 0-3 groups selected from: C₁ -C₆ alkyl, C₆ -C₁₀ aryl, heteroaryl, C₇ -C₁₁ arylalkyl, C₁ -C₆ alkylcarbonyl, C₃ -C₇ cycloalkylcarbonyl, C₁ -C₆ alkoxycarbonyl, C₇ -C₁₁ arylalkoxycarbonyl, C₁ -C₆ alkylsulfonyl or C₆ -C₁₀ arylsulfonyl;

R¹² is selected from:

H, C₁ -C₆ alkyl, triphenylmethyl, methoxyphenyldiphenylmethyl, trimethylsilylethoxymethyoxy (SEM), (C₁ -C₆ alkyl)carbonyl, (C₁ -C₆ alkoxy)carbonyl; (C₁ -C₆ alkyl)aminocarbonyl, C₃ -C₆ alkenyl, C₃ -C₇ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, aryl, heteroaryl(C₁ -C₆ alkyl)carbonyl, heteroarylcarbonyl, aryl C₁ -C₆ alkyl, (C₁ -C₆ alkyl)carbonyl, or arylcarbonyl, C₁ -C₆ alkylsulfonyl, arylsulfonyl, aryl(C₁ -C₆ alkyl)sulfonyl, heteroarylsulfonyl, heteroaryl(C₁ -C₆ alkyl)sulfonyl, aryloxycarbonyl, or aryl(C₁ -C₆ alkoxy)carbonyl, wherein said aryl groups are substituted with 0-2 substituents selected from the group consisting of C₁ -C₄ alkyl, C₁ -C₄ alkoxy, halo, CF₃, and nitro;

R¹³ is selected from: H, hydroxy, C₁ -C₁₀ alkoxy, nitro, N(R¹⁰)R¹¹, --N(R¹⁶)R¹⁷, C₁ -C₁₀ alkyl substituted with 0-3 R⁷, aryl substituted with 0-3 R⁷, heteroaryl substituted with 0-3 R⁷, or C₁ -C₁₀ alkylcarbonyl;

R¹⁴ is selected from H, C₁ -C₁₀ alkyl, C₂ -C₁₀ alkenyl, C₂ -C₁₀ alkynyl, C₁ -C₁₀ alkoxy, aryl, heteroaryl or C₁ -C₁₀ alkoxycarbonyl, CO₂ R¹⁰ or --C(═O)N(R¹⁰)R¹¹ ;

R¹⁵ is selected from: H, CO₂ R^(18a), C(═O)R^(18a), CONR^(18a) R¹⁷, --SO₂ R^(18a), --SO₂ NR^(18a) R¹⁷, C₁ -C₆ alkyl substituted with 0-1 R⁹, C₃ -C₆ alkenyl substituted with 0-1 R⁹, C₃ -C₇ cycloalkyl substituted with 0-1 R⁹, C₄ -C₁₁ cycloalkylalkyl substituted with 0-1 R⁹, aryl substituted with 0-1 R⁹ or 0-2 R⁷, or aryl(C₁ -C₆ alkyl)- substituted with 0-1 R⁹ or 0-2 R⁷ ;

R¹⁶ is selected from:

--C(═O)--O--R^(18a),

--C(═O)--R^(18b),

--C(═O)N(R^(18b))₂,

--C(═O)NHSO₂ R^(18a),

--C(═O)NHC(═O)R^(18b),

--C(═O)NHC(═O)OR^(18a),

--C(═O)NHSO₂ NHR^(18b),

--SO₂ --R^(18a),

--SO₂ --N(R^(18b))₂, or

--SO₂ --NHC(═O)OR^(18b) ;

R¹⁷ is selected from: H, C₁ -C₆ alkyl, C₃ -C₇ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, aryl, aryl(C₁ -C₆ alkyl)-, or heteroaryl(C₁ -C₆ alkyl);

R^(18a) is selected from: C₁ -C₈ alkyl, C₃ -C₁₁ cycloalkyl, aryl(C₁ -C₆ alkyl)-, (C₁ -C₆ alkyl)aryl, heteroaryl(C₁ -C₆ alkyl)-, (C₁ -C₆ alkyl)heteroaryl, biaryl(C₁ -C₆ alkyl), heteroaryl, or aryl, wherein said aryl or heteroaryl groups are optionally substituted with 0-4 R¹⁹ ;

R^(18b) is selected from R^(18a) or H;

R¹⁹ is selected from H, halogen, CF₃, CO₂ H, CN, NO₂, NR¹¹ R¹², C₁ -C₈ alkyl, C₂ -C₆ alkenyl, C₂ -C₆ alkynyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, aryl(C₁ -C₆ alkyl)-, C₁ -C₆ alkoxy, OCF₃, or C₁ -C₄ alkoxycarbonyl, aryl, --O-aryl, --SO₂ -aryl, heteroaryl, or --SO₂ -heteroaryl, wherein said aryl and heteroaryl groups may be substituted with 0-4 groups selected from hydrogen, halogen, CF₃, C₁ -C₃ alkyl, or C₁ -C₃ alkoxy;

R²⁰ is selected from hydroxy, C₁ to C₁₀ alkyloxy, C₃ to C₁₁ cycloalkyloxy, C₆ to C₁₀ aryloxy, C₇ to C₁₁ aralkyloxy, C₃ to C₁₀ alkylcarbonyloxyalkyloxy, C₃ to C₁₀ alkoxycarbonyloxyalkyloxy, C₂ to C₁₀ alkoxycarbonylalkyloxy, C₅ to C₁₀ cycloalkylcarbonyloxyalkyloxy, C₅ to C₁₀ cycloalkoxycarbonyloxyalkyloxy, C₅ to C₁₀ cycloalkoxycarbonylalkyloxy, C₇ to C₁₁ aryloxycarbonylalkyloxy, C₈ to C₁₂ aryloxycarbonyloxyalkyloxy, C₈ to C₁₂ arylcarbonyloxyalkyloxy, C₅ to C₁₀ alkoxyalkylcarbonyloxyalkyloxy, C₅ to C₁₀ (5-alkyl-1,3-dioxa-cyclopenten-2-one-yl)methyloxy, C₁₀ to C₁₄ (5-aryl-1,3-dioxa-cyclopenten-2-one-yl)methyloxy, or (R¹¹)(R¹²)N--(C₁ -C₁₀ alkoxy)-;

R²¹ is selected from: C₁ -C₈ alkyl, C₂ -C₆ alkenyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylmethyl, C₆ -C₁₀ aryl, C₇ -C₁₁ arylalkyl, or C₁ -C₁₀ alkyl substituted with 0-2 R⁷ ;

R²² is selected from:

--C(═O)--R^(18b),

--C(═O)N(R^(18b))₂,

--C(═O)NHSO₂ R^(18a),

--C(═O)NHC(═O)R^(18b),

--C(═O)NHC(═O)OR^(18a) or,

--C(═O)NHSO₂ NHR^(18b),

m is 0-2;

n is 0-4;

p is 0-2;

q is 0-4;

r is 0-2;

s is 0-1;

with the following provisos:

(1) when b is a double bond, only one of R¹⁴ or R¹⁵ is present and Q and U are not --(CH₂)--; and

(2) n, m and q are chosen such that the number of atoms connecting R¹ and Y is in the range of 8-14; and

(3) when V is -(phenyl)-Q--, then either: U is not a direct bond (i.e., U is not --(CH₂)_(n) -- where n=0) or Q is not a direct bond (i.e., Q is not --(CH₂)_(n) -- where n=0).

3! Further preferred compounds of the above invention are compounds of Formula II: ##STR12## including enantiomeric or diastereomeric forms thereof, or mixtures of enantiomeric or diastereomeric forms thereof, or pharmaceutically acceptable salt or prodrug forms thereof wherein:

b, the bond between carbon atoms numbered 4 and 5, is a carbon-carbon single or double bond;

R¹ is selected from: ##STR13## R² and R³ are independently selected from: H, C₁ -C₄ alkoxy, NR¹¹ R¹², halogen, NO₂, CN, CF₃, C₁ -C₆ alkyl, C₃ -C₆ alkenyl, C₃ -C₇ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, C₆ -C₁₀ aryl substituted with 0-2 R⁷, C₇ -C₁₁ arylalkyl, C₂ -C₇ alkylcarbonyl, or C₇ -C₁₁ arylcarbonyl;

alternatively, R² and R³ can be taken together with the carbon atoms to which they are attached to form a 5-7 membered carbocyclic or 5-7 membered heterocyclic aromatic or nonaromatic ring system, said carbocyclic or heterocyclic ring being optionally substituted with 0-2 R⁷ ;

U is selected from:

--(CH₂)_(n) --,

--N(R¹²)(CH₂)_(m) --,

--N(R¹⁰)C(═O)--, or

--C(═O)N(R¹⁰)--;

--N(R¹⁰)S(O)_(p) --, or

V is selected from:

--(CH₂)_(n) --,

--(C₁ -C₆ alkylene)-Q--, substituted with 0-3 groups independently selected from R¹³,

--(C₂ -C₇ alkenylene)-Q--, substituted with 0-3 groups independently selected from R¹³,

--(C₂ -C₇ alkynylene)-Q--, substituted with 0-3 groups independently selected from R¹³,

-(phenyl)-Q--, said phenyl substituted with 0-2 groups independently selected from R¹³,

-(pyridyl)-Q--, said pyridyl substituted with 0-2 groups independently selected from R¹³, or

-(pyridazinyl)-Q--, said pyridazinyl substituted with 0-2 groups independently selected from R¹³ ;

Q is selected from:

--(CH₂)_(n) --,

--(CH₂)_(n) O(CH₂)_(m) --,

--(CH₂)_(n) N(R¹²)(CH₂)_(m) --,

--N(R¹⁰)C(═O)--, or

--C(═O)N(R¹⁰)--;

W is selected from:

--(CH₂)_(q) C(═O)N(R¹⁰)--, or

--C(═O)--N(R¹⁰)--(CH₂)_(q) --;

X is --(CH₂)_(q) --CH(R⁸)--CH(R⁹)--;

Y i s --COR²⁰ ;

R⁶ is selected from:

H, C₁ -C₄ alkyl, hydroxy, C₁ -C₄ alkoxy, nitro, C₁ -C₆ alkylcarbonyl, --N(R¹¹)R¹², cyano, halo, CF₃, --S(O)_(p) R¹⁰, CO₂ R^(18a), CONR¹⁷ R^(18a), --COR^(18a), OR¹⁰,

C₆ to C₁₀ aryl optionally substituted with 0-3 groups selected from halogen, C₁ -C₆ alkoxy, C₁ -C₆ alkyl, CF₃, S(O)_(m) Me, or --NMe₂ ;

a heterocyclic ring system selected from pyridinyl, furanyl, thiazolyl, thienyl, pyrrolyl, pyrazolyl, triazolyl, imidazolyl, benzofuranyl, indolyl, indolinyl, quinolinyl, isoquinolinyl, benzimidazolyl, piperidinyl, tetrahydrofuranyl, pyranyl, 3H-indolyl, carbazolyl, pyrrolidinyl, piperidinyl, isoxazolinyl, isoxazolyl, or morpholinyl;

R⁷ is selected from:

H, C₁ -C₄ alkyl, hydroxy, C₁ -C₄ alkoxy, nitro, C₁ -C₄ alkylcarbonyl, --N(R¹¹)R¹², CO₂ R^(18a), SO₂ R¹¹, SO₂ NR¹⁰ R¹¹ or OR¹⁰ ;

R⁸ is selected from:

H, CONR¹⁷ R^(18a), --CO₂ R^(18a), --COR^(18a)

C₁ -C₁₀ alkyl, substituted with 0-1 R⁶,

C₂ -C₁₀ alkenyl, substituted with 0-1 R⁶,

C₂ -C₁₀ alkynyl, substituted with 0-1 R⁶,

C₃ -C₈ cycloalkyl, substituted with 0-1 R⁶,

aryl, substituted with 0-1 R⁶ or,

a heterocyclic ring system selected from pyridinyl, furanyl, thiazolyl, thienyl, pyrrolyl, pyrazolyl, triazolyl, imidazolyl, benzofuranyl, indolyl, indolinyl, quinolinyl, isoquinolinyl, benzimidazolyl, piperidinyl, tetrahydrofuranyl, pyranyl, 3H-indolyl, carbazolyl, pyrrolidinyl, piperidinyl, isoxazolinyl, isoxazolyl or morpholinyl, said heterocycle optionally substituted with 0-2 R⁷ ;

R⁹ is selected from: H or --N(R¹⁶)R¹⁷ ;

R¹⁰ is selected from H or C₁ -C₁₀ alkyl, or C₇ -C₁₀ arylalkyl;

R¹¹ is selected from hydrogen, hydroxy, C₁ to C₈ alkyl, C₃ -C₆ alkenyl, C₃ to C₁₁ cycloalkyl, C₄ to C₁₁ cycloalkylmethyl, C₁ -C₆ alkoxy, benzyloxy, C₆ to C₁₀ aryl, heteroaryl, heteroarylalkyl, C₇ to C₁₁ arylalkyl, adamantylmethyl, or C₁ -C₁₀ alkyl substituted with 0-2 R⁴ ;

alternatively, R¹⁰ and R¹¹ when both are substituents on the same nitrogen atom (as in --NR¹⁰ R¹¹) can be taken together with the nitrogen atom to which they are attached to form a heterocycle selected from:

3-azabicyclononyl, 1,2,3,4-tetrahydro-1-quinolinyl, 1,2,3,4-tetrahydro-2-isoquinolinyl, 1-piperidinyl, 1-morpholinyl, 1-pyrrolidinyl, thiamorpholinyl, thiazolidinyl or 1-piperazinyl; said heterocycle being optionally substituted with 1-3 groups selected from: C₁ -C₆ alkyl, C₆ -C₁₀ aryl, heteroaryl, C₇ -C₁₁ arylalkyl, C₁ -C₆ alkylcarbonyl, C₃ -C₇ cycloalkylcarbonyl, C₁ -C₆ alkoxycarbonyl, C₇ -C₁₁ arylalkoxycarbonyl, C₁ -C₆ alkylsulfonyl or C₆ -C₁₀ arylsulfonyl;

R¹² is selected from:

H, C₁ -C₆ alkyl, triphenylmethyl, methoxyphenyldiphenylmethyl, trimethylsilylethoxymethyoxy (SEM), C₁ -C₄ alkoxycarbonyl, C₁ -C₆ alkylcarbonyl, C₁ -C₆ alkylsulfonyl, aryl(C₁ -C₄ alkyl)sulfonyl, arylsulfonyl, aryl, heteroarylcarbonyl, or heteroarylalkylcarbonyl, wherein said aryl groups are substituted with 0-3 substituents selected from the group consisting of: C₁ -C₄ alkyl, C₁ -C₄ alkoxy, halo, CF₃, and NO₂ ;

R¹³ is selected from: H, hydroxy, C₁ -C₁₀ alkoxy, N(R¹⁰)R¹¹, --N(R¹⁶)R¹⁷, C₁ -C₁₀ alkyl substituted with 0-3 R⁷, aryl substituted with 0-3 R⁷, heteroaryl substituted with 0-3 R⁷, or C₁ -C₁₀ alkylcarbonyl;

R¹⁴ is selected from H, C₁ -C₁₀ alkyl, C₂ -C₁₀ alkenyl, C₂ -C₁₀ alkynyl, C₁ -C₁₀ alkoxy, aryl, heteroaryl or C₁ -C₁₀ alkoxycarbonyl, CO₂ R¹⁰ or --C(═O)N(R¹⁰)R¹¹ ;

R¹⁶ is selected from:

--C(═O)--O--R^(18a),

--C(═O)--R^(18b),

--SO₂ --R^(18a) or,

--SO₂ --N(18^(b))₂ ;

R¹⁷ is selected from H or C₁ -C₄ alkyl;

R^(18a) is selected from: C₁ -C₈ alkyl, C₃ -C₁₁ cycloalkyl, aryl(C₁ -C₆ alkyl)-, (C₁ -C₆ alkyl)aryl, heteroaryl(C₁ -C₆ alkyl)-, (C₁ -C₆ alkyl)heteroaryl, biaryl(C₁ -C₆ alkyl), heteroaryl, or aryl, wherein said aryl or heteroaryl groups are optionally substituted with 0-2 R¹⁹ ;

R^(18b) is selected from R^(18a) or H;

R¹⁹ is selected from H, halogen, CF₃, CO₂ H, CN, NO₂, NR¹¹ R¹², C₁ -C₈ alkyl, C₂ -C₆ alkenyl, C₂ -C₆ alkynyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, aryl(C₁ -C₆ alkyl)-, C₁ -C₆ alkoxy, OCF₃, or C₁ -C₄ alkoxycarbonyl, aryl, --O-aryl, --SO₂ -aryl, heteroaryl, or --SO₂ -heteroaryl, wherein said aryl and heteroaryl groups may be substituted with 0-4 groups selected from hydrogen, halogen, CF₃, C₁ -C₃ alkyl, or C₁ -C₃ alkoxy;

R²⁰ is selected from:

hydroxy;

C₁ to C₁₀ alkoxy;

methylcarbonyloxymethoxy-;

ethylcarbonyloxymethoxy-;

t-butylcarbonyloxymethoxy-;

cyclohexylcarbonyloxymethoxy-;

1-(methylcarbonyloxy)ethoxy-;

1-(ethylcarbonyloxy)ethoxy-;

1-(t-butylcarbonyloxy)ethoxy-;

1-(cyclohexylcarbonyloxy)ethoxy-;

i-propyloxycarbonyloxymethoxy-;

t-butyloxycarbonyloxymethoxy-;

1-(i-propyloxycarbonyloxy)ethoxy-;

1-(cyclohexyloxycarbonyloxy)ethoxy-;

1-(t-butyloxycarbonyloxy)ethoxy-;

dimethylaminoethoxy-;

diethylaminoethoxy-;

(5-methyl-1,3-dioxacyclopenten-2-on-4-yl)methoxy-;

(5-(t-butyl)-1,3-dioxacyclopenten-2-on-4-yl)methoxy-;

(1,3-dioxa-5-phenyl-cyclopenten-2-on-4-yl)methoxy- or;

1-(2-(2-methoxypropyl)carbonyloxy)ethoxy-;

R²¹ is selected from C₁ -C₈ alkyl, C₂ -C₆ alkenyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylmethyl, C₆ -C₁₀ aryl, C₇ -C₁₁ arylalkyl, or C₁ -C₁₀ alkyl substituted with 0-2 R⁴ ;

m is 0-2;

n is 0-4;

p is 0-2;

q is 0-1; and

r is 0-2;

with the following provisos:

(1) when b is a double bond, Q and U are not --(CH₂)--; and

(2) n, m and q are chosen such that the number of atoms connecting R¹ and Y is in the range of 8-14; and

(3) when V is -(phenyl)-Q--, then either: U is not a direct bond (i.e., U is not --(CH₂)_(n) -- where n=0) or Q is not a direct bond (i.e., Q is not --(CH₂)_(n) -- where n=0).

4! Still further preferred are compounds of the above invention of Formula IIIa, IIIb or IIIc: ##STR14## including enantiomeric or diasteriomeric forms thereof, or mixtures of enantiomeric or diasteriomeric forms thereof, or pharmaceutically acceptable salt or prodrug forms thereof wherein:

R¹ --U taken together are selected from: ##STR15## R² and R³ are independently selected from: H, C₁ -C₄ alkoxy, halogen, C₁ -C₆ alkyl, or C₃ -C₆ alkenyl;

V is selected from:

--(CH₂)_(n) --;

--(C₁ -C₆ alkylene)-Q--, substituted with 0-1 groups independently selected from R¹³ or,

--(C₂ -C₇ alkenylene)-Q--, substituted with 0-1 groups independently selected from R¹³, or

-(phenyl)-Q--, said phenyl substituted with 0-1 groups independently selected from R¹³,

Q is selected from:

--(CH₂)_(n) --,

--O--,

--N(R¹²)--,

--N(R¹⁰)C(═O)--, or

--C(═O)N(R¹⁰)--;

R⁷ is selected from:

H, hydroxy, C₁ -C₄ alkoxy, C₁ -C₄ alkylcarbonyl,

--N(R¹⁰)(R¹¹), CO₂ R^(18a), SO₂ N(R¹⁰)R¹¹, or OR¹⁰ ;

R⁸ is selected from:

H, CONR¹⁷ R^(18a), C₁ -C₁₀ alkyl, C₂ -C₁₀ alkenyl, C₂ -C₁₀ alkynyl, C₃ -C₈ cycloalkyl, pyridinyl, or aryl, wherein said aryl or pyridinyl groups are optionally substituted with 0-3 substituents selected from the group consisting of: C₁ -C₄ alkyl, C₁ -C₄ alkoxy, aryl, halo, cyano, CF₃, and NO₂.

R⁹ is selected from: H or --NHR¹⁶ ;

R¹⁰ is selected from H or C₁ -C₁₀ alkyl;

R¹¹ is selected from hydrogen, hydroxy, C₁ to C₈ alkyl, C₃ -C₆ alkenyl, C₃ to C₁₁ cycloalkyl, C₄ to C₁₁ cycloalkylmethyl, C₁ -C₆ alkoxy, benzyloxy, C₆ to C₁₀ aryl, heteroaryl, heteroarylalkyl, C₇ to C₁₁ arylalkyl, or adamantylmethyl;

R¹³ is selected from: H, hydroxy, C₁ -C₁₀ alkoxy, N(R¹⁰)R¹¹, --N(R¹⁶)R¹⁷, C₁ -C₁₀ alkyl substituted with 0-2 R⁷, aryl substituted with 0-3 R⁷, heteroaryl substituted with 0-2 R⁷, or C₁ -C₆ alkylcarbonyl;

R¹⁶ is selected from:

--C(═O)--O--R^(18a),

--SO₂ --R^(18a) or,

--SO₂ --NHR^(18a) ;

R^(18a) is selected from: C₁ -C₈ alkyl, C₃ -C₁₁ cycloalkyl, aryl(C₁ -C₆ alkyl)-, (C₁ -C₆ alkyl)aryl, heteroaryl(C₁ -C₆ alkyl)-, (C₁ -C₆ alkyl)heteroaryl, biaryl(C₁ -C₆ alkyl), heteroaryl, or aryl, wherein said aryl or heteroaryl groups are optionally substituted with 0-2 R¹⁹ ;

R¹⁹ is selected from: H, Br, F, Cl, CF₃, CN, NO₂, NHR¹¹, C₁ -C₄ alkyl, aryl, aryl(C₁ -C₄ alkyl)-, C₁ -C₄ alkoxy, C₁ -C₄ alkoxycarbonyl, or --O-aryl, wherein said aryl groups are optionally substituted with 0-3 substituents selected from a group consisting of halogen, CF₃, C₁ -C₃ alkyl, or C₁ -C₃ alkoxy;

R²⁰ is selected from:

hydroxy;

C₁ to C₁₀ alkoxy;

methylcarbonyloxymethoxy-;

ethylcarbonyloxymethoxy-;

t-butylcarbonyloxymethoxy-;

cyclohexylcarbonyloxymethoxy-;

1-(methylcarbonyloxy)ethoxy-;

1-(ethylcarbonyloxy)ethoxy-;

1-(t-butylcarbonyloxy)ethoxy-;

1-(cyclohexylcarbonyloxy)ethoxy-;

i-propyloxycarbonyloxymethoxy-;

t-butyloxycarbonyloxymethoxy-;

1-(i-propyloxycarbonyloxy)ethoxy-;

1-(cyclohexyloxycarbonyloxy)ethoxy-;

1-(t-butyloxycarbonyloxy)ethoxy-;

dimethylaminoethoxy-;

diethylaminoethoxy-;

(5-methyl-1,3-dioxacyclopenten-2-on-4-yl)methoxy-;

(5-(t-butyl)-1,3-dioxacyclopenten-2-on-4-yl)methoxy-;

(1,3-dioxa-5-phenyl-cyclopenten-2-on-4-yl)methoxy- or;

1-(2-(2-methoxypropyl)carbonyloxy)ethoxy-;

n is 0-4;

q is 0-1;

with the proviso that n, and q are chosen such that the number of atoms connecting R¹ and COR²⁰ is in the range of 8-14;

5! Specifically preferred compounds of the above invention are compounds of Formula I, including enantiomeric or diasteriomeric forms thereof, or mixtures of enantiomeric or diasteriomeric forms thereof, or pharmaceutically acceptable salt or prodrug forms thereof selected from the group consisting of:

3- 3- 3-(imidazolin-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid,

3- 3- 3-(imidazolin-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(n-butyloxycarbonyl-amino)propionic acid,

3- 3- 3-(imidazolin-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 3-(imidazolin-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(n-butylsulfonylamino)-propionic acid,

3- 3- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid,

3- 3- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(n-butyloxycarbonylamino)propionic acid,

3- 3- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(n-butylsulfonyl)aminopropionic acid,

3- 3- 4-(imidazolin-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid,

3- 3- 4-(imidazolin-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(n-butyloxycarbonylamino)propionic acid,

3- 3- 4-(imidazolin-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 4-(imidazolin-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(n-butylsulfonylamino)propionic acid,

3- 3- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid,

3- 3- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-5-ylcarbonyl amino!-2-(n-butyloxycarbonylamino)propionic acid,

3- 3- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(n-butylsulfonyl)aminopropionic acid,

3- 3- 3-(imidazolin-2-ylamino)propyl!isoxazolin-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid,

3- 3- 3-(imidazolin-2-ylamino)propyl!isoxazolin-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid,

3- 3- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 3-(2-aminothiazol-4-yl)propyl!isoxazolin-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 3-(2-aminothiazol-4-yl)propyl!isoxazolin-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid,

3- 3- 4-(imidazolin-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6-trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6-tritrimethylphenyl)sulfonylamino)propionic acid,

3- 3- 4-(imidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid,

3- 3- 4-(imidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(phenylsulfonylamino)-propionic acid,

3- 3- 4-(imidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((2,6,dichlorophenyl)sulfonylamino)propionic acid,

3- 3- 4-(imidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 4-(imidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((4-biphenyl)sulfonyl-amino)propionic acid,

3- 3- 4-(imidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid,

3- 3- 3-(imidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-benzyloxycarbonylamino)propionic acid,

3- 3- 3-(imidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 3-(imidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-((2,6,dichlorophenyl)sulfonylamino)propionic acid,

3- 3- 3-(imidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 3-(imidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-((4-biphenyl)sulfonylamino)propionic acid,

3- 3- 3-(imidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid,

3- 3- 2-(imidazol-2-ylamino)ethyl!isoxazolin-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid,

3- 3- 2-(imidazol-2-ylamino)ethyl!isoxazolin-5-ylcarbonylamino!-2-(phenylsulfonylamino)-propionic acid,

3- 3- 2-(imidazol-2-ylamino)ethyl!isoxazolin-5-ylcarbonylamino!-2-((2,6,dichlorophenyl)sulfonylamino)propionic acid,

3- 3- 2-(imidazol-2-ylamino)ethyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 2-(imidazol-2-ylamino)ethyl!isoxazolin-5-ylcarbonylamino!-2-((4-biphenyl)sulfonyl-amino)propionic acid,

3- 3- 2-(imidazol-2-ylamino)ethyl!isoxazolin-5-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid,

3- 3- 3-(imidazol-2-ylaminocarbonyl)propyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 3-(2-aminoimidazol-4-yl)propyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 2-(2-aminoimidazol-4-yl)ethyl!isoxazolin-5-ylmethylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 4-(benzimidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 3-(benzimidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 3-(benzimidazol-2-ylaminocarbonyl)propyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 4-(4-methylimidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 3-(4-methylimidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 4-(4,5-dimethylimidazol-2-ylamino)butyl!-isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 3-(4,5-dimethylimidazol-2-ylamino)propyl!-isoxazolin-5-ylmethylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 3-(4,5-dimethylimidazol-2-ylaminocarbonyl)propyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 4-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 3-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 4-(pyridin-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 3-(pyridin-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 3-(2-pyridin-6-yl)propyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 2-(2-aminopyridin-6-yl)ethyl!isoxazolin-5-ylmethylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 3- 3-(7-azabenzimidazol-2-yl)propyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid,

3- 5- 3-(imidazolin-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid,

3- 5- 3-(imidazolin-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(n-butyloxycarbonyl-amino)propionic acid,

3- 5- 3-(imidazolin-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 5- 3-(imidazolin-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid,

3- 5- 3-(imidazolin-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(n-butylsulfonylamino)-propionic acid,

3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid,

3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonyl amino!-2-(n-butyloxycarbonylamino)propionic acid,

3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid,

3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(n-butylsulfonyl)aminopropionic acid,

3- 5- 4-(imidazolin-2-yl amino)butyl!isoxazolin-3-ylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid,

3- 5- 4-(imidazolin-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(n -butyloxycarbonylamino)propionic acid,

3- 5- 4-(imidazolin-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 5- 4-(imidazolin-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(n-butylsulfonylamino)propionic acid,

3- 5- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid,

3- 5- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-3-ylcarbonyl amino!-2-(n-butyloxycarbonylamino)propionic acid,

3- 5- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 5- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(n-butylsulfonyl)aminopropionic acid,

3- 5- 3-(imidazol-2-yl amino)propyl!isoxazolin-3-ylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid,

3- 5- 3-(imidazolin-2-ylamino)propyl!isoxazolin-3-ylcarbonylamino!-2-(n-propyloxycarbonylamino)propionic acid,

3- 5- 3-(imidazolin-2-ylamino)propyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 5- 3-(imidazolin-2-ylamino)propyl!isoxazolin-3-ylcarbonylamino!-2-(n-propylsulfonylamino)propionic acid,

3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid,

3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonyl amino!-2-(n-propyloxycarbonylamino)propionic acid,

3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylcarbonylamino!-2-(n-propylsulfonyl)aminopropionic acid,

3- 5- 2-(imidazolin-2-ylamino)ethyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 5- 4-(pyridin-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 5- 4-(pyridin-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,6-dichlorophenylsulfonylamino)propionic acid,

3- 5- 4-(pyridin-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenyl-sulfonylamino)propionic acid,

3- 5- 4-(pyridin-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(4-biphenylsulfonylamino)propionic acid,

3- 5- 4-(pyridin-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid,

3- 5- 3-(2-aminopyridin-6-yl)propyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenyl sulfonylamino)propionic acid,

3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)-propionic acid,

3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,6-dichlorophenylsulfonylamino)propionic acid,

3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenyl-sulfonylamino)propionic acid,

3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(4-biphenylsulfonylamino)propionic acid,

3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid,

3- 5- 3-(2-aminoimidazol-4-yl)propyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)-propionic acid,

3- 5- 3-(2-aminoimidazol-4-yl)propyl!isoxazolin-3-ylcarbonylamino!-2-(2,6-dichlorophenylsulfonylamino)propionic acid,

3- 5- 3-(2-aminoimidazol-4-yl)propyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenyl sulfonylamino)propionic acid,

3- 5- 3-(2-aminoimidazol-4-yl)propyl!isoxazolin-3-ylcarbonylamino!-2-(4-biphenylsulfonylamino)propionic acid,

3- 5- 3-(2-aminoimidazol-4-yl)propyl!isoxazolin-3-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid,

3- 5- 2-(imidazol-2-ylamino)ethyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)-propionic acid,

3- 5- 2-(imidazol-2-ylamino)ethyl!isoxazolin-3-ylcarbonylamino!-2-(2,6-dichlorophenylsulfonylamino)propionic acid,

3- 5- 2-(imidazol-2-ylamino)ethyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenyl-sulfonylamino)propionic acid,

3- 5- 2-(imidazol-2-ylamino)ethyl!isoxazolin-3-ylcarbonylamino!-2-(4-biphenylsulfonylamino)propionic acid,

3- 5- 2-(imidazol-2-ylamino)ethyl!isoxazolin-3-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid,

3- 5- 3-(imidazol-2-ylaminocarbonyl)propyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid,

3- 5- 3-(benzimidazol-2-ylaminocarbonyl)propyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid,

3- 5- 4-(benzimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 5- 4-(benzimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,6-dichlorophenylsulfonylamino)propionic acid,

3- 5- 4-(benzimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid,

3- 5- 4-(benzimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(4-biphenylsulfonylamino)propionic acid,

3- 5- 4-(benzimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid,

3- 5- 4-(4-methylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 5- 4-(4-methylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,6-dichlorophenylsulfonylamino)propionic acid,

3- 5- 4-(4-methylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid,

3- 5- 4-(4-methylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(4-biphenylsulfonylamino)propionic acid,

3- 5- 4-(4-methylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid,

3- 5- 4-(4,5-dimethylimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 5- 4-(4,5-dimethylimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(2,6-dichlorophenylsulfonylamino)propionic acid,

3- 5- 4-(4,5-dimethylimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid,

3- 5- 4-(4,5-dimethylimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(4-biphenylsulfonylamino)propionic acid,

3- 5- 4-(4,5-dimethylimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid,

3- 5- 4-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 5- 4-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(2,6-dichlorophenylsulfonylamino)propionic acid,

3- 5- 4-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid,

3- 5- 4-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(4-biphenylsulfonylamino)propionic acid,

3- 5- 4-(4-,5,6,7-tetrahydrobenzimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid,

3- 5- 3-(7-azabenzimidazol-2-yl)propyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid,

3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2- (2,6-dimethyl-4-phenyl)phenylsulfonylamino!propionic acid,

3- 5- 4-(4-methylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,6-dimethyl-4-phenyl)phenylsulfonylamino!propionic acid,

3- 5- 4-(4,5-dimethylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2- (2,6-dimethyl-4-phenyl)phenylsulfonylamino!propionic acid,

3- 5- 4-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2- (2,6-dimethyl-4-phenyl)phenylsulfonylamino!propionic acid,

3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2- (2,6-dichloro -4-phenyl)phenyl sulfonylamino!propionic acid,

3- 5- 4-(4-methylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,6-dichloro -4-phenyl)phenylsulfonylamino!propionic acid,

3- 5- 4-(4,5-dimethylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2- (2,6-dichloro -4-phenyl)phenylsulfonylamino!propionic acid,

3- 5- 4-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2- (2,6-dichloro-4-phenyl)phenylsulfonylamino!propionic acid,

3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-3-(phenylsulfonylmethyl)propionic acid,

3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-3-(1-adamantylmethylaminocarbonyl)propionic acid,

3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-3-(3-pyridinyl)propionic acid,

3- 3- 3-(imidazolin-2-yl amino)propyloxy!isoxazol-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid,

3- 3- 3-(imidazolin-2-ylamino)propyloxy!isoxazol-5-yl carbonyl amino!-2-(n-butyloxycarbonyl-amino)propionic acid,

3- 3- 3-(imidazolin-2-ylamino)propyloxy!isoxazol-5-yl carbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 3-(imidazolin-2-ylamino)propyloxy!isoxazol-5-yl carbonyl amino!-2-(n-butylsulfonylamino)-propionic acid,

3- 3- 3-(tetrahydropyrimid-2-ylamino)propyloxy!-isoxazol-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid,

3- 3- 3-(tetrahydropyrimid-2-ylamino)propyloxy!-isoxazol-5-ylcarbonyl amino!-2-(n-butyloxycarbonylamino)propionic acid,

3- 3- 3-(tetrahydropyrimid-2-ylamino)propyloxy!-isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 3-(tetrahydropyrimid-2-ylamino)propyloxy!-isoxazol-5-yl carbonylamino!-2-(n-butylsulfonyl)aminopropionic acid,

3- 3- 2-(imidazolin-2-yl amino)ethyloxy!isoxazol-5-yl carbonylamino!-2-(benzyloxycarbonylamino)-propionic acid,

3- 3- 3-(imidazolin-2-ylamino)ethyloxy!isoxazol-5-yl carbonylamino!-2-(n-butyloxycarbonylamino)propionic acid,

3- 3- 3-(imidazolin-2-ylamino)ethyloxy!isoxazol-5-yl carbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 3-(imidazolin-2-ylamino)ethyloxy!isoxazol-5-ylcarbonylamino!-2-(n-butylsulfonylamino)propionic acid,

3- 3- 3-(tetrahydropyrimid-2-yl amino)ethyloxy!-isoxazol-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid,

3- 3- 3-(tetrahydropyrimid-2-ylamino)ethyloxy!-isoxazol-5-ylcarbonylamino!-2-(n-butyloxycarbonylamino)propionic acid,

3- 3- 3-(tetrahydropyrimid-2-ylamino)ethyloxy!-isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 3-(tetrahydropyrimid-2-ylamino)ethyloxy!-isoxazol-5-ylcarbonylamino!-2-(n-butylsulfonylamino)propionic acid,

3- 3- 3-(imidazol-2-ylamino)propyloxy!isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 3-(benzimidazol-2-ylamino)propyloxy!isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 3-(4-methylimidazol-2-ylamino)propyloxy!-isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 3-(4,5-dimethylimidazol-2-ylamino)propyloxy!-isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 3-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)propyloxy!-isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 3-(pyridin-2-ylamino)propyloxy!isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

3- 3- 3-(imidazol-2-ylaminocarbonyl)ethoxy!isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid,

In the present invention it has been discovered that the compounds of Formula I above are useful as inhibitors of cell-matrix and cell-cell adhesion processes. The present invention includes novel compounds of Formula I and methods for using such compounds for the prevention or treatment of diseases resulting from abnormal cell adhesion to the extracellular matrix which comprises administering to a host in need of such treatment a therapeutically effective amount of such compound of Formula I.

In the present invention it has also been discovered that the compounds of Formula I above are useful as inhibitors of α_(v)β₃. The compounds of the present invention inhibit the binding of vitronectin to α_(v) β₃ and inhibit cell adhesion.

The present invention also provides pharmaceutical compositions comprising a compound of Formula I and a pharmaceutically acceptable carrier.

The compounds of Formula I of the present invention are useful for the treatment (including prevention) of angiogenic disorders. The term "angiogenic disorders" as used herein includes conditions involving abnormal neovascularization, such as tumor metastasis and ocular neovascularization, including, for example, diabetic retinopathy, neovascular glaucoma, age-related macular degeneration, and retinal vein occlusion, comprising administering to a mammal in need of such treatment a therapeutically effective amount of a compound of Formula I described above.

The compounds of Formula I of the present invention may be useful for the treatment or prevention of other diseases which involve cell adhesion processes, including, but not limited to, inflammation, bone degradation, thromboembolic disorders, restenosis, rheumatoid arthritis, asthma, allergies, adult respiratory distress syndrome, graft versus host disease, organ transplantation rejection, septic shock, psoriasis, eczema, contact dermatitis, osteoporosis, osteoarthritis, atherosclerosis, inflammatory bowel disease and other autoimmune diseases. The compounds of Formula I of the present invention may also be useful for wound healing.

The term "thromboembolic disorders" as used herein includes conditions involving platelet activation and aggregation, such as arterial or venous cardiovascular or cerebrovascular thromboembolic disorders, including, for example, thrombosis, unstable angina, first or recurrent myocardial infarction, ischemic sudden death, transient ischemic attack, stroke, atherosclerosis, venous thrombosis, deep vein thrombosis, thrombophlebitis, arterial embolism, coronary and cerebral arterial thrombosis, myocardial infarction, cerebral embolism, kidney embolisms, pulmonary embolisms, or such disorders associated with diabetes, comprising administering to a mammal in need of such treatment a therapeutically effective amount of a compound of Formula I described above.

The compounds of the present invention may be used for other ex vivo applications to prevent cellular adhesion in biological samples.

The compounds of the present invention can also be administered in combination with one or more additional therapeutic agents selected from: anti-coagulant or coagulation inhibitory agents, such as heparin or warfarin; anti-platelet or platelet inhibitory agents, such as aspirin, piroxicam, or ticlopidine; thrombin inhibitors such as boropeptides, hirudin or argatroban; or thrombolytic or fibrinolytic agents, such as plasminogen activators, anistreplase, urokinase, or streptokinase.

The compounds of Formula I of the present invention can be administered in combination with one or more of the foregoing additional therapeutic agents, thereby to reduce the doses of each drug required to achieve the desired therapeutic effect. Thus, the combination treatment of the present invention permits the use of lower doses of each component, with reduced adverse, toxic effects of each component. A lower dosage minimizes the potential of side effects of the compounds, thereby providing an increased margin of safety relative to the margin of safety for each component when used as a single agent. Such combination therapies may be employed to achieve synergistic or additive therapeutic effects for the treatment of thromboembolic disorders.

By "therapeutically effective amount" it is meant an amount of a compound of Formula I that when administered alone or in combination with an additional therapeutic agent to a cell or mammal is effective to prevent or ameliorate the thromboembolic disease condition or the progression of the disease.

By "administered in combination" or "combination therapy" it is meant that the compound of Formula I and one or more additional therapeutic agents are administered concurrently to the mammal being treated. When administered in combination each component may be administered at the same time or sequentially in any order at different points in time. Thus, each component may be administered separately but sufficiently closely in time so as to provide the desired therapeutic effect.

The term anti-coagulant agents (or coagulation inhibitory agents), as used herein, denotes agents that inhibit blood coagulation. Such agents include warfarin (available as COUMADIN™) and heparin.

The term anti-platelet agents (or platelet inhibitory agents), as used herein, denotes agents that inhibit platelet function such as by inhibiting the aggregation, adhesion or granular secretion of platelets. Such agents include the various known non-steroidal anti-inflammatory drugs (NSAIDS) such as aspirin, ibuprofen, naproxen, sulindac, indomethacin, mefenamate, droxicam, diclofenac, sulfinpyrazone, and piroxicam, including pharmaceutically acceptable salts or prodrugs thereof. Of the NSAIDS, aspirin (acetylsalicyclic acid or ASA), and piroxicam. Piroxicam is commercially available from Pfizer Inc. (New York, N.Y.), as FELDANE™. Other suitable anti-platelet agents include ticlopidine, including pharmaceutically acceptable salts or prodrugs thereof. Ticlopidine is also a preferred compound since it is known to be gentle on the gastro-intestinal tract in use. Still other suitable platelet inhibitory agents include thromboxane-A2-receptor antagonists and thromboxane-A2-synthetase inhibitors, as well as pharmaceutically acceptable salts or prodrugs thereof.

The phrase thrombin inhibitors (or anti-thrombin agents), as used herein, denotes inhibitors of the serine protease thrombin. By inhibiting thrombin, various thrombin-mediated processes, such as thrombin-mediated platelet activation (that is, for example, the aggregation of platelets, and/or the granular secretion of plasminogen activator inhibitor-1 and/or serotonin) and/or fibrin formation are disrupted. Such inhibitors include boroarginine derivatives and boropeptides, hirudin and argatroban, including pharmaceutically acceptable salts and prodrugs thereof. Boroarginine derivatives and boropeptides include N-acetyl and peptide derivatives of boronic acid, such as C-terminal α-aminoboronic acid derivatives of lysine, ornithine, arginine, homoarginine and corresponding isothiouronium analogs thereof. The term hirudin, as used herein, includes suitable derivatives or analogs of hirudin, referred to herein as hirulogs, such as disulfatohirudin. Boropeptide thrombin inhibitors include compounds described in Kettner et al., U.S. Pat. No. 5,187,157 and European Patent Application Publication Number 293 881 A2, the disclosures of which are hereby incorporated herein by reference. Other suitable boroarginine derivatives and boropeptide thrombin inhibitors include those disclosed in PCT Application Publication Number 92/07869 and European Patent Application Publication Number 471 651 A2, the disclosures of which are hereby incorporated herein by reference, in their entirety.

The phrase thrombolytics (or fibrinolytic) agents (or thrombolytics or fibrinolytics), as used herein, denotes agents that lyse blood clots (thrombi). Such agents include tissue plasminogen activator, anistreplase, urokinase or streptokinase, including pharmaceutically acceptable salts or prodrugs thereof. Tissue plasminogen activator (tPA) is commercially available from Genentech Inc., South San Francisco, Calif. The term anistreplase, as used herein, refers to anisoylated plasminogen streptokinase activator complex, as described, for example, in European Patent Application No. 028,489, the disclosures of which are hereby incorporated herein by reference herein, in their entirety. Anistreplase is commercially available as EMINASE™. The term urokinase, as used herein, is intended to denote both dual and single chain urokinase, the latter also being referred to herein as prourokinase.

Administration of the compounds of Formula I of the invention in combination with such additional therapeutic agent, may afford an efficacy advantage over the compounds and agents alone, and may do so while permitting the use of lower doses of each. A lower dosage minimizes the potential of side effects, thereby providing an increased margin of safety.

The compounds of the present invention are also useful as standard or reference compounds, for example as a quality standard or control, in tests or assays involving the binding of vitronectin or fibrinogen to α_(v) β₃. Such compounds may be provided in a commercial kit, for example, for use in pharmaceutical research involving α_(v) β₃. The compounds of the present invention may also be used in diagnostic assays involving α_(v) β₃.

The compounds herein described may have asymmetric centers. Unless otherwise indicated, all chiral, diastereomeric and racemic forms are included in the present invention. Many geometric isomers of olefins, C═N double bonds, and the like can also be present in the compounds described herein, and all such stable isomers are contemplated in the present invention. It will be appreciated that compounds of the present invention that contain asymmetrically substituted carbon atoms may be isolated in optically active or racemic forms. It is well known in the art how to prepare optically active forms, such as by resolution of racemic forms or by synthesis, from optically active starting materials. All chiral, diastereomeric, racemic forms and all geometric isomeric forms of a structure are intended, unless the specific stereochemistry or isomer form is specifically indicated.

When any variable (for example but not limited to, R², R⁴, R⁶, R⁷, R⁸, R¹², and R¹⁴, n, etc.) occurs more than one time in any constituent or in any formula, its definition on each occurrence is independent of its definition at every other occurrence. Thus, for example, if a group is shown to be substituted with 0-2 R⁴, then said group may optionally be substituted with up to two R⁴ and R⁴ at each occurrence is selected independently from the defined list of possible R⁴. Also, by way of example, for the group --N(R^(5a))₂, each of the two R^(5a) substituents on N is independently selected from the defined list of possible R^(5a). Similarly, by way of example, for the group --C(R⁷)₂ --, each of the two R⁷ substituents on C is independently selected from the defined list of possible R⁷.

When a bond to a substituent is shown to cross the bond connecting two atoms in a ring, then such substituent may be bonded to any atom on the ring. When a bond joining a substituent to another group is not specifically shown or the atom in such other group to which the bond joins is not specifically shown, then such substituent may form a bond with any atom on such other group.

When a substituent is listed without indicating the atom via which such substituent is bonded to the rest of the compound of Formula I, then such substituent may be bonded via any atom in such substituent. For example, when the substituent is piperazinyl, piperidinyl, or tetrazolyl, unless specified otherwise, said piperazinyl, piperidinyl, tetrazolyl group may be bonded to the rest of the compound of Formula I via any atom in such piperazinyl, piperidinyl, tetrazolyl group.

Combinations of substituents and/or variables are permissible only if such combinations result in stable compounds. By stable compound or stable structure it is meant herein a compound that is sufficiently robust to survive isolation to a useful degree of purity from a reaction mixture, and formulation into an efficacious therapeutic agent.

The term "substituted", as used herein, means that any one or more hydrogen on the designated atom is replaced with a selection from the indicated group, provided that the designated atom's normal valency is not exceeded, and that the substitution results in a stable compound. When a substitent is keto (i.e., ═O), then 2 hydrogens on the atom are replaced.

As used herein, "alkyl" is intended to include both branched and straight-chain saturated aliphatic hydrocarbon groups having the specified number of carbon atoms (for example, "C₁ -C₁₀ " denotes alkyl having 1 to 10 carbon atoms); "haloalkyl" is intended to include both branched and straight-chain saturated aliphatic hydrocarbon groups having the specified number of carbon atoms, substituted with 1 or more halogen (for example --C_(v) F_(w) where v=1 to 3 and w=1 to (2v+1)); "alkoxy" represents an alkyl group of indicated number of carbon atoms attached through an oxygen bridge; "cycloalkyl" is intended to include saturated ring groups, including mono-,bi- or poly-cyclic ring systems, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, and adamantyl; and "biycloalkyl" is intended to include saturated bicyclic ring groups such as 3.3.0!bicyclooctane, 4.3.0!bicyclononane, 4.4.0!bicyclodecane (decalin), 2.2.2!bicyclooctane, and so forth. "Alkenyl" is intended to include hydrocarbon chains of either a straight or branched configuration and one or more unsaturated carbon-carbon bonds which may occur in any stable point along the chain, such as ethenyl, propenyl and the like; and "alkynyl" is intended to include hydrocarbon chains of either a straight or branched configuration and one or more triple carbon-carbon bonds which may occur in any stable point along the chain, such as ethynyl, propynyl and the like.

The terms "alkylene", "alkenylene", "phenylene", and the like, refer to alkyl, alkenyl, and phenyl groups, respectively, which are connected by two bonds to the rest of the structure of Formula I. Such "alkylene", "alkenylene", "phenylene", and the like, may alternatively and equivalently be denoted herein as "-(alkyl)-", "-(alkyenyl)-" and "-(phenyl)-", and the like.

"Halo" or "halogen" as used herein refers to fluoro, chloro, bromo and iodo; and "counterion" is used to represent a small, negatively charged species such as chloride, bromide, hydroxide, acetate, sulfate and the like.

As used herein, "aryl" or "aromatic residue" is intended to mean phenyl or naphthyl; the term "arylalkyl" represents an aryl group attached through an alkyl bridge.

As used herein, "carbocycle" or "carbocyclic residue" is intended to mean any stable 3- to 7-membered monocyclic or bicyclic or 7- to 14-membered bicyclic or tricyclic or an up to 26-membered polycyclic carbon ring, any of which may be saturated, partially unsaturated, or aromatic. Examples of such carbocyles include, but are not limited to, cyclopropyl, cyclopentyl, cyclohexyl, phenyl, biphenyl, naphthyl, indanyl, adamantyl, or tetrahydronaphthyl (tetralin).

As used herein, the term "heterocycle" or "heterocyclic" is intended to mean a stable 5- to 7-membered monocyclic or bicyclic or 7- to 10-membered bicyclic heterocyclic ring which may be saturated, partially unsaturated, or aromatic, and which consists of carbon atoms and from 1 to 4 heteroatoms independently selected from the group consisting of N, O and S and wherein the nitrogen and sulfur heteroatoms may optionally be oxidized, and the nitrogen may optionally be quaternized, and including any bicyclic group in which any of the above-defined heterocyclic rings is fused to a benzene ring. The heterocyclic ring may be attached to its pendant group at any heteroatom or carbon atom which results in a stable structure. The heterocyclic rings described herein may be substituted on carbon or on a nitrogen atom if the resulting compound is stable. Examples of such heterocycles include, but are not limited to, pyridyl (pyridinyl), pyrimidinyl, furanyl (furyl), thiazolyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, tetrazolyl, benzofuranyl, benzothiophenyl, indolyl, indolenyl, isoxazolinyl, isoxazolyl, quinolinyl, isoquinolinyl, benzimidazolyl, piperidinyl, 4-piperidonyl, pyrrolidinyl, 2-pyrrolidonyl, pyrrolinyl, tetrahydrofuranyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, decahydroquinolinyl or octahydroisoquinolinyl, azocinyl, triazinyl, 6H-1,2,5-thiadiazinyl, 2H,6H-1,5,2-dithiazinyl, thianthrenyl, pyranyl, isobenzofuranyl, chromenyl, xanthenyl, phenoxathiinyl, 2H-pyrrolyl, pyrrolyl, imidazolyl, pyrazolyl, isothiazolyl, isoxazolinyl, isoxazolyl, oxazolyl, pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, indolizinyl, isoindolyl, 3H-indolyl, indolyl, 1H-indazolyl, purinyl, 4H-quinolizinyl, isoquinolinyl, quinolinyl, phthalazinyl, naphthyridinyl, quinoxalinyl, quinazolinyl, cinnolinyl, pteridinyl, 4aH-carbazole, carbazole, β-carbolinyl, phenanthridinyl, acridinyl, perimidinyl, phenanthrolinyl, phenazinyl, phenarsazinyl, phenothiazinyl, furazanyl, phenoxazinyl, isochromanyl, chromanyl, pyrrolidinyl, pyrrolinyl, imidazolidinyl, imidazolinyl, pyrazolidinyl, pyrazolinyl, piperidinyl, piperazinyl, indolinyl, isoindolinyl, quinuclidinyl, morpholinyl or oxazolidinyl. Also included are fused ring and spiro compounds containing, for example, the above heterocycles.

At used herein, the term "heteroaryl" refers to aromatic heterocyclic groups. Such heteroaryl groups are preferably 5-6 membered monocylic groups or 8-10 membered fused bicyclic groups. Examples of such heteroaryl groups include, but are not limited to pyridyl (pyridinyl), pyrimidinyl, furanyl (furyl), thiazolyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, indolyl, isoxazolyl, oxazolyl, pyrazinyl, pyrimidinyl, pyridazinyl, benzofuranyl, benzothienyl, benzimidazolyl, quinolinyl, or isoquinolinyl.

As used herein, "pharmaceutically acceptable salts" refer to derivatives of the disclosed compounds wherein the parent compound of Formula I is modified by making acid or base salts of the compound of Formula I. Examples of pharmaceutically acceptable salts include, but are not limited to, mineral or organic acid salts of basic residues such as amines; alkali or organic salts of acidic residues such as carboxylic acids; and the like.

"Prodrugs" are considered to be any covalently bonded carriers which release the active parent drug according to Formula I in vivo when such prodrug is administered to a mammalian subject. Prodrugs of the compounds of Formula I are prepared by modifying functional groups present in the compounds in such a way that the modifications are cleaved, either in routine manipulation or in vivo, to the parent compounds. Prodrugs include compounds of Formula I wherein hydroxyl, amino, sulfhydryl, or carboxyl groups are bonded to any group that, when administered to a mammalian subject, cleaves to form a free hydroxyl, amino, sulfhydryl, or carboxyl group respectively. Examples of prodrugs include, but are not limited to, acetate, formate and benzoate derivatives of alcohol and amine functional groups in the compounds of Formula I, and the like. Examples of representative carboxyl and amino prodrugs are included under the definition of R², R³, and Y.

The pharmaceutically acceptable salts of the compounds of Formula I include the conventional non-toxic salts or the quaternary ammonium salts of the compounds of Formula I formed, for example, from non-toxic inorganic or organic acids. For example, such conventional non-toxic salts include those derived from inorganic acids such as hydrochloric, hydrobromic, sulfuric, sulfamic, phosphoric, nitric and the like; and the salts prepared from organic acids such as acetic, propionic, succinic, glycolic, stearic, lactic, malic, tartaric, citric, ascorbic, pamoic, maleic, hydroxymaleic, phenylacetic, glutamic, benzoic, salicylic, sulfanilic, 2-acetoxybenzoic, fumaric, toluenesulfonic, methanesulfonic, ethane disulfonic, oxalic, isethionic, and the like.

The pharmaceutically acceptable salts of the present invention can be synthesized from the compounds of Formula I which contain a basic or acidic moiety by conventional chemical methods. Generally, the salts are prepared by reacting the free base or acid with stoichiometric amounts or with an excess of the desired salt-forming inorganic or organic acid or base in a suitable solvent or various combinations of solvents.

The pharmaceutically acceptable salts of the acids of Formula I with an appropriate amount of a base, such as an alkali or alkaline earth metal hydroxide e.g. sodium, potassium, lithium, calcium, or magnesium, or an organic base such as an amine, e.g., dibenzylethylenediamine, trimethylamine, piperidine, pyrrolidine, benzylamine and the like, or a quaternary ammonium hydroxide such as tetramethylammoinum hydroxide and the like.

As discussed above, pharmaceutically acceptable salts of the compounds of the invention can be prepared by reacting the free acid or base forms of these compounds with a stoichiometric amount of the appropriate base or acid, respectively, in water or in an organic solvent, or in a mixture of the two; generally, nonaqueous media like ether, ethyl acetate, ethanol, isopropanol, or acetonitrile are preferred. Lists of suitable salts are found in Remington's Pharmaceutical Sciences, 17th ed., Mack Publishing Company, Easton, Pa., 1985, p. 1418, the disclosure of which is hereby incorporated by reference.

The disclosures of all of the references cited herein are hereby incorporated herein by reference in their entirety.

Synthesis

The compounds of the present invention can be prepared in a number of ways well known to one skilled in the art of organic synthesis. The compounds of the present invention can be synthesized using the methods described below, together with synthetic methods known in the art of synthetic organic chemistry, or variations thereon as appreciated by those skilled in the art. Preferred methods include, but are not limited to, those described below. All references cited herein are hereby incorporated in their entirety herein by reference.

Compounds of Formula I wherein the central heterocycle is a 3,5-disubstituted isoxazoline ring can be conveniently prepared by dipolar cycloaddition of nitrile oxides with appropriate dipolarophiles (for reviews of 1,3-dipolar cycloaddition chemistry, see 1,3-Dipolar Cycloaddition Chemistry (Padwa, ed.), Wiley, New York, 1984; Kanemasa and Tsuge, Heterocycles 1990, 30, 719). The requisite nitrile oxides are in turn prepared from the corresponding aldehydes via the intermediate oximes.

Scheme I illustrates one synthetic sequence which will provide the 3,5-isoxazolines of this invention. An appropriately substituted hydroxylamine is treated with NCS in DMF according to the method of Liu, et al. (J. Org. Chem. 1980, 45, 3916). The resulting hydroximinoyl chloride is then dehydrohalogenated in situ using TEA to give a nitrile oxide, which undergoes a 1,3-dipolar cycloaddition to a suitably substituted alkene to afford the isoxazoline. Alternatively, the oxime may be oxidatively chlorinated, dehydrochlorinated and the resulting nitrile oxide trapped by a suitable alkene under phase transfer conditions according to the method of Lee (Synthesis 1982, 508).

Subsequent hydrolysis of the ester using conventional methods known to one skilled in the art of organic synthesis gives the desired acids. Coupling of the resulting acids to appropriately substituted α- or β-amino esters affords an intermediate which can be deprotected to give compounds of Formula I. The coupling is carried out using any of the many methods for the formation of amide bonds known to one skilled in the art of organic synthesis. These methods include but are not limited to conversion of the acid to the corresponding acid chloride, or use of standard coupling procedures such as the azide method, mixed carbonic acid anhydride (isobutyl chloroformate) method, carbodiimide (dicyclohexylcarbodiimide, diisopropylcarbodiimide, or water-soluble carbodiimides) method, active ester (p-nitrophenyl ester, N-hydroxysuccinic imido ester) method, carbonyldiimidazole method, phosphorus reagents such as BOP-Cl. Some of these methods (especially the carbodiimide) can be enhanced by the addition of 1-hydroxybenzotriazole. ##STR16##

Alternately, as depicted in Scheme Ia, the above sequence can be carried out on an aldehyde bearing a suitably protected functional group which can be converted into R¹ after elaboration of the right hand side of the target molecules. ##STR17##

Additional isoxazolinyl acetates useful as starting materials for the preparation of compounds of Formula I, wherein V is -(phenyl)-Q-- and Q is other than a single bond, can be prepared by cycloaddition of a suitably substituted chloro or bromooxime with an ester of vinyl acetic acid as shown in Scheme Ib using literature methods or modifications thereof. (D. P. Curran & J. Chao, J. Org. Chem., 1988, 53, 5369-71; J. N. Kim & E. K. Ryu, Heterocycles, 1990, 31, 1693-97). ##STR18##

The compounds of the present invention wherein Y is an oxyalkoxy group, e.g. alkoxycarbonyloxyalkoxy, may be prepared by reacting a suitably protected carboxylic acid of Formula I with an e.g. an alkoxycarbonyloxyalkyl chloride in the presence of an iodide source, such as tetrabutylammonium iodide or potassium iodide, and an acid scavenger, such as triethylamine or potassium carbonate, using procedures known to those skilled in the art.

The appropriately substituted racemic β-amino acids may be purchased commercially or, as is shown in Scheme II, Method 1, prepared from the appropriate aldehyde, malonic acid and ammonium acetate according to the procedure of Johnson and Livak (J. Am. Chem. Soc. 1936, 58, 299). Racemic β-substituted-β-amino esters may be prepared through the reaction of dialkylcuprates or alkyllithiums with 4-benzoyloxy-2-azetidinone followed by treatment with anhydrous ethanol (Scheme I, Method 2) or by reductive amination of β-keto esters as is described in published PCT patent application W09316038. (Also see Rico et al., J. Org. Chem. 1993, 58, 7948-51.) Enantiomerically pure β-substituted-β-amino acids can be obtained through the optical resolution of the racemic mixture or can be prepared using numerous methods, including: Arndt-Eistert homologation of the corresponding α-amino acids as shown in Scheme II, Method 3 (see Meier, and Zeller, Angew Chem. Int. Ed. Engl. 1975, 14, 32; Rodriguez, et al. Tetrahedron Lett. 1990, 31, 5153; Greenlee, J. Med. Chem. 1985, 28, 434 and references cited within); and through an enantioselective hydrogenation of a dehydroamino acid as is shown in Scheme II, Method 4 (see Asymmetric Synthesis, Vol. 5, (Morrison, ed.) Academic Press, New York, 1985). A comprehensive treatise on the preparation of β-amino acid derivatives may be found in published PCT patent application WO 9307867, the disclosure of which is hereby incorporated by reference. ##STR19##

The synthesis of N² -substituted diaminopropionic acid derivatives can be carried out via Hoffman rearrangement of a wide variety of asparagine derivatives as described in Synthesis, 266-267, (1981).

The dipolarophiles used to prepare the compounds of this invention may be prepared by numerous methods. The ω-alkenoic ester class of dipolarophile may be purchased commercially or prepared by oxidation of the corresponding ω-alkenols by the method of Corey and Schmidt (Tetrahedron Lett. 1979, 399, Scheme III). ##STR20##

Synthesis of compounds of Formula I which incorporate the isoxazoline ring in the reverse orientation, i.e., a 5,3-disubstituted isoxazoline ring, is shown in Scheme IV. Cycloaddition of an appropriately substituted alkene with t-butylformyloxime using the method described by Gree et al. (Bioorganic and Med. Chem. Lett., 1994, 253) provides the intermediate t-butyl 5-substituted isoxazolin-3-yl!acetate. This ester can be converted to compounds of Formula I using the methods described herein. ##STR21##

Alternately, as illustrated in Scheme IVa, the reverse isoxazolines may be prepared by reaction of an appropriate nitro ester with an appropriately substituted alkene in the presence of a suitable dehydrating agent such as phenylisocyanate or phosphorus oxychloride in the presence of an organic amine base, such as triethylamine or diisopropylethylamine. ##STR22##

N-protected aminoalkenes useful in the synthesis of compounds of this invention can be prepared from the commercially available alcohols as shown in Scheme IVb, via reaction with a suitable activating agent such as p-toluenesulfonyl chloride in the presence of a base such as pyridine, followed by displacement with sodium azide in a suitable solvent such as DMF. Reduction of the azide by the action of triphenylphosphine in the presence of water (for example see, Scriven, E. F. V., Turnbull, K., Chemical Rev. 1988, 88, 297-360, and the references therein) provides an amine which is suitably protected, for example, Fmoc, Boc or phthalimide group according to literature procedures. (Protecting Groups in Organic Synthesis 2nd Ed. Green, T. W., Wits, P. G. M. pp 309-406. 1991 John Wiley & Sons, Inc. New York) ##STR23##

The appropriate nitroesters are available from commercial sources or can be synthesized according to literature methods (Seebach, D. et al., Chem. Ber. 1982, 115, 1705-1720; Chaser. D. W., Syn. Comm. 1982, 841-842).

Additional methods for the preparation of compounds of the present invention containing the isoxazoline ring in the reverse orientaion are outlined in Scheme V. An appropriate ω-alkenol can be reacted with commercially available ethyl chorooximidoacetate in a suitable solvent, such as tetrahydrofuran or methylene chloride, in the presence of a suitable base, such as aqueous sodium bicarbonate or triethylamine, to provide the isoxazoline. Alternately the same intermediate is prepared by heating the alkenol in the presence of diethylnitromalonate in refluxing mesitylene or decalin, by the method of Shimizu et al. (Bull. Chem. Soc. Jpn. 1985, 58, 2519-2522.) Oxidation of theresulting alcohol the corresponding aldehyde can be achieved by numerous methods described in the literature (for example see Comprehensive Organic Transformations by Larock, R. C., p 604, 605, 607-613. VCH publishers, New York, N.Y., 1989). Reductive amination of the intermediate aldehyde (for suitable methods see, Abdel-Magid, A. F., Maryanoff, C. A., and Carson, K. G., Tetrahedron Lett., 1990, 31, 5595-5598, and references contained therein) with a variety of heteroaryl amines, which may additionally contain suitable protecting groups, provides the substituted amines. Alternatively, depending on the nature of the heterocyclic amine, the reductive amination can be carried out in a two step procedure, wherein initial formation of an imine is carried out by treatment of the aldehyde with the desired amine in the presence of a dehydrating agent such as magnesium sulfate, sodium sulfate, or molecular sieves, in a suitable solvent such as carbon tetrachloride, methylene chloride, benzene or toluene (for example see, Modern Synthetic Reactions 2nd ed. House, H. O., Benjamin/Cummings Publishing Co, Menlo Park, Calif., 1972.). The imine is then subsequently reduced with a variety of reducing agents such as sodium borohydride, sodium cyanoborohydride, or sodium triacetoxyborohydride, in a suitable solvent such as methanol, ethanol, tetrahydrofuran, dioxane or 1,2-dichloroethane, to provide the desired amines.

Hydrolysis of the ester using conventional methods known to one skilled in the art of organic synthesis provides acid intermediates. Coupling of the resulting acids to the appropriately substituted α- or β-amino ester is accomplished using standard coupling reagents, as described above. The esters may be saponified or in the case of tert-butyl esters the acid may be produced either by the action of trifluoroacetic acid with or without an inert solvent such as methylene chloride, or by the action of anhydrous HC1 in a solvent such as ether or dioxane. Additional protecting groups may be removed by methods known to one skilled in the art (for example see, Protective Groups in Organic Synthesis 2nd, ed. Greene, T. W., and Wuts, P. G. M., John Wiley & Sons, Inc. New York, 1991). ##STR24##

A convenient preparation of suitably protected 2-aminoimidazoles is outlined in Scheme Va. ##STR25##

Compounds of formula I wherein b is a double bond can be prepared using one of the routes depicted in Scheme VI. Bromination followed by subsequent dehydrobromination of a suitably substituted methyl 3-(cyanophenyl)isoxazolin-5-ylacetate, prepared as described above, using the method of Elkasaby & Salem (Indian J. Chem., 1980, 19B, 571-575) provides the corresponding isoxazole intermediate. Alternately, this intermediate can be obtained by 1,3-dipolar cycloaddition of a cyanophenylnitrile oxide (prepared from the corresponding chlorooxime as described in Scheme I) with an appropriate alkyne to give the isoxazole directly. Hydrolysis of the ester using conventional methods known to one skilled in the art of organic synthesis provides the acid intermediates. Coupling of the resulting acids to an appropriately substituted α- or β-amino ester is accomplished using standard coupling reagents, as described above. Saponification gives the acids. ##STR26## Compounds of Formula I wherein b is a double bond and Q is oxygen can be prepared from commercially available methyl 3-hydroxy-5-isoxazolecarboxylate as illustrated in Scheme VII. Coupling of the hydroxy group to a suitably N-protected amino alcohol can be achieved in one step under Mitsunobu reaction conditions (Hughs, D. L.; Organic Reactions, Volume 42, John Wiley and Sons, 1992, pages 335-656). Alternately, a two step process of activation of the N-protected aminoalcohol as a aryl or alkyl sulfonate ester or by conversion to halide followed by alkylation of the hydroxyisoxazole gives the same result. Bases suitable for this reaction include alkaline hydrogen carbonates, alkaline carbonates, cesium carbonate, alkaline hydrides, and alkaline alcoholates such as sodium ethoxide and potassium t-butoxide. The reaction can be run in a number of different solvents including lower alkyl and branched alcohols, ethereal solvents, or halocarbons, but it proceeds most readily in polar aprotic solvents such as DMF and DMSO. Saponification of the ester using standard conditions known to one skilled in the art provides an acid intermediate which can be converted using the methods described above into compounds of Formula I. ##STR27##

Additional aldehydes useful for the preparation of compounds of formula I in the methods depicted in schemes I-VII can be prepared as illustrated in Scheme VIII below: ##STR28##

Heterocyclic alkenes and aldehydes useful as intermediates for the preparation of compounds of formula I in the methods depicted in Schemes I-VII can be prepared as illustrated in Scheme VIIIa and VIIIb. The carboxylic acids prepared in scheme III, can be converted to an acid halide, by a variety of methods, such as treatment with oxalyl chloride or thionyl chloride either neat or in the presence of a suitable solvent such as methylene chloride or toluene, as outlined in the literature (for example, see Comprehensive Organic Transformations by Larock, R. C., p 964-965. VCH publishers, New York, N.Y., 1989). Treatment of the acid chloride with diazomethane in a suitable solvent such as ether, or dioxane, to form the diazoketone, followed by treatment with HBr (for example, see Comprehensive Organic Transformations by Larock, R. C., p 346. VCH publishers, New York, N.Y., 1989), provides versatile intermediates for the synthesis of many heterocycles. The examples shown in scheme VIIIa, are for illustration purposes and do not constitute a limitation on the scope of the invention. For example, as illustrated in method A, the α-haloketone can be treated with N-acetylguanidine in a suitable solvent such as acetonitrile from room temperature to reflux, or N,N-dimethylformamide from room temperature to 80° C. according to the method of Little, T. L., and Webber, S. E. (J. Org. Chem., 1994, 59, 7299-7305.) to provide a 2-amino-4-imidazole derivative. Alternatively, treatment of the α-haloketone with thiourea, in the presence of a suitable solvent such as toluene or acetone, at a temperature from 20° C. to the boiling point of the solvent, according to the method of Patt, W. C., Skeean, R. W., and Steinbaugh, B. A., (Synth. Comm. 1990, 20, 3097-3102), provides the analogous 2-amino-5-thiazole derivative. The alkenes can be converted by a hydroboration-oxidation procedure (for example, see Comprehensive Organic Transformations by Larock, R. C., p 497-498. VCH publishers, New York, N.Y., 1989), to provide the alcohols. The alcohols can be oxidized to the corresponding aldehydes by numerous published methods (for example see Comprehensive Organic Transformations by Larock, R. C., 604, 605, 607-613. VCH publishers, New York, N.Y., 1989). ##STR29##

Synthesis of pyridyl-containing alkenes and aldehydes, proceeds as depicted in Scheme VIIIb. The amino group of 2-amino-6-methylpyridine is protected by treatment with 2,6-hexanedione, followed by deprotonation of the methyl group with lithium diisopropylamide according to the method of Breukelman, S. P., Meakins, G. D., and Tirel, M. D. (J. Chem. Soc. Chem. Comm. 1982, 800-801.). The lithio intermediate can be trapped with a variety of electrophiles such as formaldehyde, ethylene oxide or 3-(tertbutyldimethylsilyloxy)-1-bromopropane to provide the alcohol intermediates. Oxidation of the alcohol to an aldehyde as described as described in detail above, followed by olefination reaction under any of a number of known conditions, such as, for example, a Wittig reaction or treatment with various titanium reagents provides the alkene intermediates (see Comprehensive Organic Transformations by Larock, R. C., p 173-184. VCH publishers, New York, N.Y., 1989). ##STR30##

Alternately, reductive amination of the appropriate aldehyde intermediates with heterocyclic amines as shown in method A and method B of Scheme VIIIc, using methods described above, yields the desired amine intermediates. Hydroboration-oxidation of the double bond, followed by oxidation of the alcohol (vide supra) provides additional aldehyde intermediates useful for the synthesis of compounds of this invention. For heterocyclic amines unstable to the hydrogen peroxide required in the hydroboration oxidation procedure, the reductive amination can be carried out on appropriate esterified ω-hydroxy aldehydes, as outlined in method B. Hydrolysis of the esters and oxidation of the alcohol provides the aldehyde. ##STR31##

Compounds of Formula I wherein R¹ is 2-iminopyrrolidinyl, 2-iminopiperidinyl, or 2-iminoazepinyl can be prepared from the commercially available imides as outlined in Scheme IX. ##STR32##

Additional compounds of formula I where R⁹ is --N(R¹⁶)R¹⁷ can be prepared from the compounds of Schemes I, IA, IV, IVa, and IVb, wherein R¹⁶ is Cbz (benzyloxycarbonyl), is shown in Scheme X. Selective removal of the Cbz group may be accomplished by hydrogenation using palladium suspended on barium sulfate as the catalyst in a suitable solvent such as methanol or ethanol, with or without a co-solvent, by the method of Nikam, S. S., Kornberg, B. E., Johnson, D. R., and Doherty, A. M. (Tetrahedron Lett. 1995, 36, 197-200). Using this method, the Cbz group can be removed with minimal to no cleavage of the N--O bond contained in the isozazoline rings shown in Scheme X example A, and Scheme X example B.

The resulting amines can be converted to additional compound of formula I by treatment with a wide variety of reagents, for example, acyl halides, chloroformares, isocyanates, sulfonylchlorides, chlorosulfonamides, and sulfonylisocyanates, etc. using standard methods. ##STR33##

The detailed processes for preparing the compounds of Formula I are illustrated by the following Examples. It is, however, understood that this invention is not limited to the specific details of these examples. Melting points are uncorrected. Proton nuclear magnetic resonance spectra (¹ H NMR) were measured in chloroform-d (CDCl₃) unless otherwise specified and the peaks are reported in parts per million (ppm) downfield from tetramethylsilane (TMS). The coupling patterns are reported as follows: s, singlet; d, doublet; t, triplet; q, quartet; qt, quintet; m, multipier.

EXAMPLE 2 3- 3- 3-(N-3,4,5,6-Tetrahydropyrimidin-2-yl)aminopropyl!-(5R,S)-isoxazoline-5-yl!methylcarbonylamino-2-benzyloxycarbonylaminopropionic acid

A. 3- 3- 3-(N-3,4,5,6-Tetrahydropyrimidin-2-yl)aminopropyl!-(5R,S)-isoxazoline-5-yl!methylcarbonylamino-2-benzyloxycarbonylaminopropionic acid

The compound of Ex. 16, Part G (199 mg; 0.5 mmol), methyl 3-amino-2-benzyloxycarbonylaminopropionate 147 mg (0.5 mmol), and triethylamine (100 mg; 1 mmol) in 3 ml dimethylformamide was treated with (177 mg; 0.55 mmol) of O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate (TBTU) and the mixture was stirred at room temperature for 18 hours. TLC indicated no starting material; the volatiles were removed under high vaccum. The residue was purified by flash chromatography; 55 g silica gel column using 8% MeOH:CHCl₃ followed by 20% to afford the desired product as a white solid (252 mg; 79.9% yield). NMR indicated contamination with triethylamine salt. The compound will be used in the next step without further purification. HRMS calcd. for C₂₄ H₃₄ N₆ O₆ ( M+H!⁺): 503.261808; found: 503.259832.

B. 3- 3- 3-(N-3,4,5,6-Tetrahydropyrimidin-2-yl)aminopropyl!-(5R, S)-isoxazoline-5-yl!methylcarbonylamino-2-benzyloxycarbonylaminopropionic acid

A mixture of the compound of Ex. 2, Part A (100 mg; 0.159 mmol) and lithium hydroxide (12 mg; 0.5 mmol) in 2 ml of a 1:1 methanol:water was stirred at room temperature for one hour. TLC indicated dissappearance of starting material. The mixture was diluted with water and washed with hexane. The aqueous layer was neutralized with 1N HCl (0.5 mmol) and then stripped. The residue was purified on a LH20 size exclusion column using 100% methanol as an eluent. The product obtained was lyophilyzed from 2 ml 1N HCl followed by 2 ml distilled water. The desired product was obtained as an off-white solid (59 mg; 70.7% yield). ¹ H NMR (300 MHz CDCl₃): 1.721-1.785 (m, 4H); 2.294-2.408 (m, 3H); 2.499 (dd, 1H, J₁ =14.28 Hz, J₂ =6.59 Hz); 2.675 (dd, 1H, J₁ =17.2 Hz, J₂ =6.23 Hz); 2.984 (dd, 1H, J₁ =17.2 Hz, J₂ =10.25 Hz); 3.125 (t, 2H, J=6.59 Hz); 3.225 (m, 4H); 3.343-3.558 (m, 2H); 4.214 (m, 1H); 4.768 (m, 1H); 4.973 (s, 2H); 7.145-7.230 (m, 5H). HRMS calcd. for C₂₃ H₃₂ N₆ O₆ ( M+H!⁺): 489.246158; found: 489.247644.

EXAMPLE 16 3- 3- 3-(N-3,4,5,6-Tetrahydropyrimidin-2-yl)aminopropyl!-(5R,S)-isoxazolin-5-yl!methylcarbonylamino-2-phenylsulfonylaminopropionic acid

A. N-(4-Hydroxybutyl)phthalimide:

A solution of 4-amino-1-butanol (5.616 g; 63 mmol) and triethylamine (12.3 ml; 88.2 mmol) in 130 ml tetrahydrofuran was treated with N-carbethoxyphthalimide (13.82 g; 63 mmol). The mixture was refluxed for 18 hours. TLC showed the formation of product (1:1 Ethyl acetate:Hexane Rf=0.3). The mixture was diluted with ethyl acetate and washed with water. The aqueous layer was extracted with more ethyl acetate and the organic layers combined, dried (MgSO₄), filtered, concentrated and the residue purified by flash chromatography; 200 g silica gel column using 2:3 ethyl acetate:Hexane followed by 1:1 to provide N-(4-hydroxybutyl)phthalimide as a white solid (9.108 g; 65.9% yield). ¹ H NMR (300 MHz, CDCl₃): 1.426 (t, 2H, J=4.93 Hz); 1.597-1.663 (m, 2H); 1.738-1.813 (m, 2H); 3.668-3.768 (m, 4H); 7.715 (m, 2H); 7.838 (m, 2H).

B. N-(4-Oxobutyl)phthalimide:

Oxalyl Chloride (4.01 ml; 46 mmol) in 90 ml dichloromethane was cooled at -78° C. in a dry ice-acetone bath. Dimethylsulfoxide (4.26 ml; 60 mmol) in 22 ml dichloromethane was then added dropwise and the mixture stirred at -78° C. for 30 minutes. N-(4-Hydroxybutyl)phthalimide (9.108 g; 41.5 mmol) in 45 ml dichloromethane was then added and the mixture stirred in the -78° C. bath for 45 minutes. The mixture was then warmed in a 0° C. ice bath and stirred for one hour. Triethylamine (23 g; 230 mmol) in 23 ml dichloromethane was then added and the stirred for an additional 30 minutes. The mixture was worked up by washing with water. The organic layer was separated, dried (MgSO₄), filtered, concentrated and the residue purified by flash chromatography; 200 g silica gel column using 1:3 ethyl acetate:Hexane to provide N-(4-oxobutyl)phthalimide as a white solid (7.469 g; 82.8% yield). ¹ H NMR (300 MHz, CDCl₃): 2.023 (m, 2H); 2.546 (dt, 2H, J₁ =7.324 Hz, J₂ =1.098 Hz); 3.749 (t, 2H, J=6.958 Hz); 7.734 (m, 2H); 7.845 (m, 2H); 9.777 (t, 1H, J=1.099 Hz).

C. 4-(N-Phthaloyl)aminobutyraldehyde oxime:

N-(4-oxobutyl)phthalimide (7.46 g; 34.3 mmol) and triethylamine (17.2 g; 172 mmol) in 75 ml ethanol was treated with hydroxylamine hydrochloride (11.95 g; 172 mmol) and stirred at room temperature for 2 hours. TLC indicated no starting material. The solvent was stripped off and the mixture diluted with ethyl acetate and washed with water. The organic layer was dried (MgSO₄), filtered, concentrated and the residue dried in vacuo to afford 4-(N-phthaloyl)aminobutyraldehyde oxime (7.469 g; 73.9% yield). A 2:1 mixture of isomers was obtained and the following is data on the major isomer. ¹ H NMR (300 MHz, CDCl₃): 1.856-1.956 (m, 2H); 2.409-2.479 (dt, 2H, J₁ =7.691 Hz, J₂ =5.493 Hz); 3.713-3.762 (t, 2H, J=7.324 Hz); 6.769 (t, 1H, J=5.493 Hz); 7.720 (m, 2H); 7.836 (m, 2H).

D. tert-Butyl 3- 3-(N-Phthaloyl)aminopropyl!-(5R,S)-isoxazoline-5-yl acetate:

N-Chlorosuccinimide (3.39 g; 25.4 mmol) and 1 drop of pyridine in 50 ml chloroform was treated with 4-(N-phthaloyl)aminobutyraldehyde oxime (5.89 g; 25.4 mmol) in 25 ml chloroform added over a 5 minute period. After the mixture was completely in solution, it was stirred at room temperature for 1.5 hours. NMR was used to monitor the dissappearance of starting material. The mixture was treated with tert-butyl-3-butenoate (5.42 g; 38.1 mmol) followed by triethylamine 2.70 g (26.7 mmol) added dropwise over a 2 hour period. The mixture was stirred at room temperature for 18 hours and worked up by washing with water, drying the organic layer (MgSO₄), filtering, and concentrating. The residue was purified by flash chromatography; 200 g silica gel using 1:5 Ethyl acetate:Hexane followed by 1:3 to provide t-Butyl 3- 3-(N-Phthaloyl)aminopropyl!-(5R,S)-isoxazoline-5-yl acetate (7.469 g; 63.7% yield). ¹ H NMR (300 MHz, CDCl₃): 1.430 (s, 9H); 1.967 (m, 2H); 2.355-2.476 (m, 3H); 2.624-2.723 (m, 2H); 3.103 (dd, 1H, J₁ =16.85 Hz, J₂ =10.25 Hz); 3.730 (t, 2H, J=6.958 Hz); 4.820-4.879 (m, 1H); 7.712 (m, 2H); 7.813 (m, 2H).

E. tert-Butyl 3-(3-aminopropyl)-(5R,S)-isoxazoline-5-yl acetate:

tert-Butyl 3- 3-(N-phthaloyl)aminopropyl!-(5R,S)-isoxazoline-5-yl acetate (6.025 g; 16.2 mmol) in 200 ml ethanol was treated with hydrazine and the mixture stirred at room temperature for 18 hours. A thick white precipitate that had formed was filtered off and washed with more ethanol. The mother liquor was stripped and diluted with chloroform and washed with water. The organic layer was separated, dried (MgSO₄), filtered, concentrated and the residue (3.811 g) purified by flash chromatography; 250 g silica gel column using 10% methanol:chloroform to elute impurities and then 1:1 methanol:chloroform to provide t-Butyl 3-(3-aminopropyl)-(5R,S)-isoxazoline-5-yl acetate (1.0 g; 25.5% yield). ¹ H NMR (300 MHz, CDCl₃): 1.398 (bs, 2H); 1.457 (s, 9H); 1.727 (m, 2H); 2.379-2.489 (m, 3H); 2.659-2.784 (m, 4H); 3.114 (dd, 1H, J₁ =17.21 Hz, J₂ =10.25 Hz); 4.816-4.919 (m, 1H). HRMS calcd. for C₁₂ H₂₂ N₂ O₃ ( M+H!⁺): 243.170868; found: 234.170966.

F. tert-Butyl 3- 3-(N-3,4,5,6-tetrahydropyrimidin-2-yl)aminopropyl!-(5R,S)-isoxazoline-5-ylacetate:

(tert-Butyl 3-(3-aminopropyl)-(5R,S)-isoxazoline-5-yl acetate 990 mg (4.09 mmol) in 15 ml pyridine was treated with 2-Methylthio-3,4,5,6-tetrahydropyrimidine hydroiodide 1.135 g (4.4 mmol) and the mixture stirred at reflux for 22 hours. TLC indicated no starting material. The mixture was stripped and pumped. The residue was purified by flash chromatography; 130 g silica gel column using 2% MeOH:CHCl₃ followed by 4% and finally 6% to elute 923 mg of t-Butyl 3- 3-(N-3,4,5,6-tetrahydropyrimidin-2yl)aminopropyl!-(5R,S)-isoxazoline-5-ylacetate (49.9% yield). ¹ H NMR (300 MHz, CDCl₃): 1.460 (s, 9H); 1.897-2.001 (m, 4H); 2.435 (t, 2H, J=6.226 Hz); 2.523 (dd, 1H, J₁ =15.75 Hz, J₂ =6.59 Hz); 2.662 (dd, 1H, J₁ =16.11 Hz, J₂ =6.59 Hz); 2.779 (dd, 1H, J₁ =17.40 Hz, J₂ =7.69 Hz); 3.177 (dd, 1H, J₁ =17.40 Hz, J₂ =10.25 Hz); 3.299 (dt, 2H); 3.400 (m, 4H); 4.844-4.949 (m, 1H); 7.518 (s, 2H), 7.623 (t, 1H, J=6.23 Hz). HRMS calcd. for C₁₆ H₂₈ N₄ O₃ ( M+H!⁺): 325.223966; found: 325.223355.

G. 3- 3-(N-3,4,5,6-tetrahydropyrimidin-2-yl)aminopropyl!-(5R,S)-isoxazoline-5-ylacetic acid:

tert-Butyl 3- 3-(N-3,4,5,6-tetrahydropyrimidin-2-yl)aminopropyl!-(5R,S)-isoxazoline-5-ylacetate (885 mg; 1.96 mmol) was treated with 1:1 dichloromethane:trifluoroacetic acid (20 ml) and stirred at room temperature for one hour. TLC indicated no starting material. The mixture was stripped and pumped to afford 3- 3-(N-3,4,5,6-tetrahydropyrimidin-2yl)aminopropyl!-(5R,S)-isoxazoline-5-ylacetic acid as a brown solid (777 mg; 100% yield). ¹ H NMR (300 MHz DMSO-d6): 1.694 (m, 2H); 1.804 (m, 2H); 2.302 (t, 2H, J=7.32 Hz); 2.511 (d, 2H, J=6.59 Hz); 2.681 (dd, 1H, J₁ =17.21 Hz, J₂ =7.32 Hz); 3.037-3.152 (m, 3H); 3.231 (m, 4H); 4.693-4.794 (m, 1H); 7.456 (t, 1H, J=5.13 Hz); 7.788 (s, 2H). HRMS calcd. for C₁₂ H₂₀ N₄ O₃ ( M+H!⁺): 269.161366; found: 269.161204.

H. Methyl 3- 3- 3-(N-3,4,5,6-tetrahydropyrimidin-2-yl)aminopropyl!-(5R,S)-isoxazoline-5-yl!methylcarbonylamino-2-phenylsulfonylaminopropionate:

A solution of the compound of Ex. 16, part G (199 mg; 0.5 mmol), methyl 3-amino-2-phenylsulfonylaminopropionate (147 mg; 0.5 mmol), and triethylamine (100 mg; 1 mmol) in 3 ml dimethylformamide was treated with 265 mg (0.6 mmol) of benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (BOP Reagent) and the mixture stirred at room temperature for 18 hours. TLC indicated no starting material; the mixture was pumped to remove most of the dimethylformamide. The residue was purified by flash chromatography; 75 g silica gel column using 15% methanol:chloroform to elute the desired product. NMR indicated contamination with triethylamine salt and some form of the BOP Reagent. The compound was then purified on a LH20 size exclusion column using 100% methanol as the eluent. 113 mg of desired product was obtained with slight contamination from triethylamine salts (35.3% yield). This product was taken on to the next step without further purification.

I. 3- 3- 3-(N-3,4,5,6-Tetrahydropyrimidin-2-yl)aminopropyl!-(5R,S)-isoxazoline-5-yl!methylcarbonylamino-2-phenylsulfonylaminopropionic acid:

A mixture of the compound of Ex. 16, Part H (107 mg; 0.168 mmol) and lithium hydroxide (14 mg; 0.6 mmol) in 2 ml of a 1:1 methanol:water was stirred at room temperature for one hour. TLC indicated dissappearance of the starting material. The mixture was diluted with water and washed with hexane. The aqueous layer was neutralized with 1N HCl (0.6 mmol) and then stripped. The residue was purified on a LH20 size exclusion column using 100% methanol as eluent. The product obtained was lyophilyzed from 2 ml 1N HCl followed by 2 ml distilled water. The desired product was obtained as an off-white solid (68 mg; 76.2% yield). ¹ H NMR (300 MHz CDCl₃): 1.646-1.797 (m, 4H); 2.244 (m, 3H); 2.322-2.403 (m, 1H); 3.005 (t, 2H, J=6.96 Hz); 3.153-3.196 (m, 6H); 3.318 (d, 1H, J=5.86 Hz); 3.424 (dd, 1H, J₁ =13.73 Hz, J₂ =4.39 Hz); 3.835 (m, 1H); 4.693 (m, 1H); 7.303-7.429 (m, 3H); 7.660 (m, 2H). HRMS calcd. for C₂₁ H₃₀ N₆ O₆ S ( M+H!⁺): 495.202580; found: 495.201869.

EXAMPLE 56 2-benzyloxycarbonylamino-3- 3- 4- (N-imidazolin-2-yl)amino!butyl!-(5R,S)-isoxazolin-5-yl!carbonylamino!propionic acid

A. 5-Phthalimidopentanol:

A mixture of 10.317 g (100 mmol) 5-amino-1-pentanol and 14.812 g (100 mmol) phthalic anhydride in 200 mL toluene was stirred 18 h under nitrogen at reflux while employing a Dean-Stark trap for removal of water. The reaction was allowed to cool to room temperature and solvent was removed. The residue was flash column chromatographed (1;1 hexanes-ethyl acetate) to provide 19.77 g (84.0 mmol, 84%) of a clear liquid; NMR(CDCl₃): 7.66-7.88 (m, 4H), 3.59-3.75 (m, 4H), 1.32-1.79 (m, 6H); Mass spectrum: m/z 234 (M+H).

B. 5-Phthalimidopentanal:

A solution of 260 mL methylene chloride and 10.39 mL (108.22 mmol) oxalyl chloride was stirred in a 1000 mL round bottom flask under nitrogen at -78° C. Added over 10 min was 16 mL dimethyl sulfoxide. Next added over 5 min was 23.61 g (101.21 mmol) of the product obtained from Ex. 56, Step A in 60 mL methylene chloride and the mixture stirred for 15 min. Next added was 60 mL (325.0 mmol) triethylamine and the mixture allowed to warm to room temperature. The mixture was poured into water, extracted with three portions of methylene chloride which were combined, dried, filtered and stripped of solvent to provide 21.22 g (91.7 mmol, 90%) of a clear liquid; NMR(CDCl₃): 9.76 (t, 1H), 7.68-7.90 (m, 4H), 3.73 (t, 2H), 2.50 (t, 2H), 1.60-1.81 (m, 4H); Mass spectrum: m/z 232 (M+H).

C. 5-phthalimidopentanal oxime:

A mixture of 20.60 g (89.08 mmol) of the product obtained from Ex. 56, Step B, 250 mL pyridine and 12.27 g (2 equivs) of hydroxylamine hydrochloride was stirred 18 hr under nitrogen at room temperature. Solvent was removed and the residue triturated under water. The resulting solid was filtered and suction dried to provide 12.22 g (49.62 mmol, 55%) of a white solid, mp=120°-123° C.; NMR(CDCl₃): 7.69-7.90 (m, 4H), 6.70 and 7.40 (two t, 1H), 7.03 (bs, 1H), 1.50-3.77 (m, 8H); Mass spectrum: m/z 247 (M+H).

D. tert-Butyl-3- 4-phthalimidobutyl!-isoxazolin-5-(R,S)-yl)-carboxylate:

A mixture of 3.50 g (14.212 mmol) of the product obtained from Ex. 56, Step C, 100 mL N,N-dimethylformamide and 1.897 g (14.212 mmol) N-chlorosuccinimide were stirred for 3 h at room temperature under nitrogen. Solvent was removed and the residue flash column chromatographed (2:1 hexanes-ethyl acetate) to provide 3.50 g (12.46 mmol, 87%) of a clear liquid; NMR(CDCl₃): 8.50 (bs, 1H), 7.69-7.88(m, 4H), 3.70 (m, 2H), 2.58 (m, 2H), 1.70 (m, 4H); Mass spectrum: m/z 262 ((M+H)-H2O). A mixture of 3.50 g (12.46 mmol) of the product thus obtained, 50 mL tetrahydrofuran, 25 mL water, 3.0 g (excess) t-butyl acrylate and 3.0 g (excess) sodium bicarbonate was stirred 48 h at room temperature under nitrogen. The mixture was poured into water and extracted with three portions of ethyl acetate. The combined organic layers were dried over anhydrous magnesium sulfate, filtered and solvent removed. The residue was flash column chromatographed (3:2 hexanes-ethyl acetate) to provide 2.98 g (8.00 mmol, 64%) of a clear liquid; NMR(CDCl₃): 7.70-7.86 (m, 4H), 4.83 (m, 1H), 3.72 (t, 2H), 3.15 (m, 2H), 2.42 (t, 2H), 1.60-1.82 (m, 4H), 1.48 (s, 9H); Mass spectrum: m/z 373 (M+H).

E. tert-Butyl-3- 4- (N-imidazolin-2-yl)amino!butyl!-(5R,S)-isoxazolin-5-ylcarboxylate, hydroiodide:

A mixture of 2.92 g (7.80 mmol) of the product obtained from Ex. 56, Part D, 100 mL absolute ethanol and 0.75 mL (3 ecluivs) hydrazine was stirred for 18 h at room temperature under nitrogen. Water was added until all dissolved. The mixture was extracted with three portions of ethyl acetate. The combined organic layers were dried over anhydrous magnesium sulfate, filtered and solvent was removed. To the residue was added 1.904 g (7.80 mmol) 2-methylthio-4,5-dihydroimidazole hydroiodide and 100 mL pyridine. The mixture was set at reflux under nitrogen for 18 h. The mixture was allowed to cool to room temperature and the residue flash column chromatographed (1:4 methanol-chloroform) to provide 0.48 g (1.95 mmol, 25 %) of a gum; NMR(CDCl₃): 7.90 (bs, 1H), 7.33 (bs, 1H), 4.90 (m, 1H), 1.63-3.80 (m, 14H), 1.47 (s, 9H); Mass spectrum: m/z 311 (free base+H).

F. 3- 4- (N-imidazolin-2-yl)amino!butyl!-(5R,S)-isoxazolin-5-ylcarboxylic acid, trifluoracetate:

A mixture of 480 mg (1.95 mmol) of the product obtained from Ex. 56, Part E, 15 mL methylene chloride and 1.0 mL (excess) trifluoroacetic acid was stirred for 18 h at room temperature under nitrogen. Solvent was removed and toluene was added. Solvent was removed to provide 240 mg (0.629 mmol, 32 %) of a gum; NMR(d₆ -DMSO): 8.27 (m, 1H), 7.20 (m, 1H), 4.90 (m, 1H), 1.40-3.70 (m, 14H); Mass spectrum: m/z 255 (M+H).

G. tert-Butyl 2-benzyloxycarbonylamino-3- 3- 4- (N-imidazolin-2-yl)amino!butyl!-(5R,S)-isoxazolin-5-yl!carbonylaminopropionate:

A mixture of 230 mg (0.603 mmol) of the product obtained from Ex. 56, Part F, 217.8 mg (0.740 mmol) (R)-t-butyl-3-amino-2-benzyloxycarbonylaminopropionate, 180 mg (0.930 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide and 26 mg (catalytic) 1-hydroxybenzotriazole hydrate was stirred at room temperature under nitrogen. Added was 10 mL N,N-dimethylformamide followed by 170 mg (1.67 mmol) triethylamine and the mixture stirred 18 h at room temperature under nitrogen. Solvent was removed and the residue flash column chromatographed (1:4 methanol/chloroform) to provide 217 mg (0.329 mmol, 54%) of a gum; NMR(CDCl₃ /TMS): 8.36 (bs, 1H), 7.68 (bs, 1H), 7.58 (bs, 1H), 7.34 (s, 5H), 6.01 (t, 1H), 5.10 (s, 2H), 4.87 (m, 1H), 1.50-4.38 (m, 17H), 1.41 (s, 9H); Mass spectrum: m/z 531 (free base+H).

H. 2-benzyloxycarbonylamino-3- 3- 4- (N-imidazolin-2-yl)amino!butyl!-(5R,S)-isoxazolin-5-yl!carbonylaminopropionic acid, trifluoroacetate:

A mixture of 217 mg (0.329 mmol) of the product obtained from Ex. 56, Step H, 50 mL methylene chloride and 50 mL of 0.2M NaOH was placed in a separatory funnel, shaken, and the layers separated. The organic layer was washed two more times with 50 mL portions of 0.2M NaOH. The organic layer was dried over anhydrous magnesium sulfate, filtered and solvent was removed. To the residue was added 10 mL methylene chloride and 0.5 mL (excess) trifluoroacetic acid and the mixture stirred 18 h at room temperature under nitrogen. Solvent was removed and toluene was added. Solvent was removed and the residue triturated under hexanes. The resulting solid was filtered to dryness to provide 127 mg (0.215 mmol, 65%) of the title compound as an off-white solid, mp=100°-6° C.; NMR(d₆ -DMSO): 7.21-8.35 (m, 10H), 1.50-5.12 (m, 20H); Mass spectrum: m/z 475 (M+H).

EXAMPLE 83 2(S)-Benzyloxycarbonylamino-3- 3-(4-(N- 3,4,5,6-tetrahydropyrimidin-2-yl!amino)butyl)isoxazolin-5-(R,S)-ylcarbonyl!aminopropionic acid

The title compound was prepared in an analogous manner to the compound of Example 56 by substitution of 2-methylthio-3,4,5,6-tetrahydropyrimidine hydroiodide for 2-methylthio-4,5-dihydroimidazole hydroiodide in Ex. 56, Part E. mp 101°-108° C.

EXAMPLE 110 2(S)-Benzyloxycarbonylamino-3- 3-(3-(N- 3,4,5,6-tetrahydropyrimidin-2-yl!amino)propyl)isoxazolin-5-(R,S)-ylcarbonyl!aminopropionic acid

A. 4-Phthalimidobutyraldehyde oxime:

A solution of 4-phthalimidobutyraldehyde (R. Hamilton et al., Tetrahedron Letters, 1993, 34, 2847) (17.38 g, 80 mmol) in pyridine (150 mL) was treated with hydroxylamine hydrochloride (6.67 g, 96 mmol) and stirred at room temperature for 17 h. After concentration, the residue was triturated in water, stirred for 3 h, and filtered to provide the title product as a light tan solid (14.15 g, 76%): NMR (CDCl₃) δ 8.06 (b, 1H), 7.85 (m, 2H), 7.70 (m, 2H), 7.46 (t, 0.15H), 6.76 (t, 0.85H), 3.73 (t, 2H), 2.44 (m, 1.7H), 2.28 (m, 0.3H), 1.90 (m, 2H); mass spec (NH₃ -CI) m/z 233 (M+H⁺, 100%).

B. tert-Butyl 3-(3- 3-phthalimidopropyl!-isoxazolin-5-(R,S)-yl)-carboxylate:

A mixture of the product of Ex. 110, Part A (2.10 g, 9.05 mmol), N-chlorosuccinimide (1.21 g, 9.05 mmol), pyridine (2 drops), t-butyl acrylate (2.7 mL, 18.10 mmol), and triethylamine (1.5 mL, 10.86 mmol) in 30 mL chloroform was reacted according to the procedure of Ex. 284, Part D to provide the title product (2.40 g, 74%): NMR (CDCl₃) δ 7.84 (m, 2H), 7.78 (m, 2H), 4.82 (m, 1H), 3.78 (t, 2H), 3.20 (m, 2H), 2.41 (t, 2H), 2.02 (m, 2H), 1.44 (S, 9H); mass spec (NH₃ -CI) m/z 376 (M+NH₄ ⁺, 100%).

C. 3-(3- 3-phthalimidopropyl!isoxazolin-5-(R,S)-yl)-carboxylic acid:

The product of Ex. 110 step B (500 mg, 1.40 mmol) was reacted with trifluoroacetic acid (5 mL) in 10 mL methylene chloride according to the procedure of Ex. 284, Part E to provide 420 mg (100%) of the title product as a foamy solid: NMR (DMSO-d₆) δ 7.81 (m, 2H), 7.78 (m, 2H), 5.40 (b, 1H), 5.02 (m, 1H), 3.79 (t, 2H), 3.30 (m, 2H), 2.42 (t, 2H), 2.00 (q, 2H).

D. tert-Butyl N² -benzyloxycarbonyl-N³ - 3- 3-(3-phthalimidopropyl)isoxazolin-5-(R,S)-yl!carbonyl!-2-(S)-2,3-diaminopropionate:

The product of Ex. 110, Part C (420 mg, 1.40 mmol) was reacted with t-butyl N² -benzyloxycarbonyl-2-(S)-2,3-diaminopropionate (412 mg, 1.40 mmol), O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate (450 mg, 1.40 mmol), triethylamine (0.6 mL, 4.20 mmol) in 25 mL ethyl acetate according to the procedure of Ex. 284, Part F to provide 595 mg (66%) of the title product: NMR (CDCl₃) δ 7.81 (m, 2H), 7.70 (m, 2H), 7.34 (s, 5H), 7.04 (b, 1H), 5.06 (s, 2H), 4.90 (m, 1H), 4.38 (m, 1H), 3.70 (m, 4H), 3.20 (m, 3H), 2.39 (bt, 2H), 1.98 (m, 2H), 1.40 (s, 9H); mass spec (ESI) m/z 579.4 (M+H⁺, 100%).

E. tert-Butyl N² -benzyloxycarbonyl-N³ - 3- 3-(3-aminopropyl)isoxazolin-5-(R,S)-yl!carbonyl!-2-(S)-2,3-diaminopropionate:

The product of Ex. 110 step D (550 mg, 0.99 mmol) was reacted with hydrazine (0.1 mL, 2.50 mmol) in 5 mL ethanol according to the procedure of Ex. 284 Part G to provide 223 mg (50%) of the title product: NMR (CDCl₃) δ 7.38 (m, 5H), 7.04 (b, 1H), 5.80 (dd, 1H), 5.10 (s, 2H), 4.90 (m, 1H), 4.38 (m, 1H), 3.64 (m,2H), 3.40-3.12 (m, 2H), 2.76 (m ,2H), 2.40 (m,2H), 1.72 (m, 2H), 1.50 (s, 9H), 1.46 (b, 2H); mass spec (ESI) m/z 449.5 (M+H⁺, 100%).

F. tert-Butyl N² -benzyloxycarbonyl-N³ - 3-(3-(N- 3,4,5,6-tetrahydropyrimidine-2-yl!amino)propyl)isoxazolin-5-(R,S)-ylcarbonyl!-(S)-2,3-diaminopropionate:

The product of Ex. 110, step E (124 mg, 0.276 mmol) was reacted with 2-methylthio-3,4,5,6-tetrahydropyrimidine hydroiodide (86.0 mg, 0.332 mmol) in 2 mL pyridine according to the procedure of Ex. 284 Part H to provide 30 mg (25%) of the title product: NMR (CDCl₃) δ 7.80 (b, 1H), 7.38 (m, 5H), 7.18 (b, 2H), 5.82-5.78 (2b, 1H), 5.10 (s,2H), 4.90 (m, 1H), 4.38 (b, 2H), 3.80 (b, 2H), 3.58-3.10 (m, 9H), 2.42 (b, 2H), 1.95 (b, 2H), 1.42 (s,9H); mass spec (ESI) m/z 531.4 (M+H⁺, 100%).

G. N2-benzyloxycarbonyl-N³ - 3-(3-(N- 3,4,5,6-tetrahydropyrimidine-2-yl!amino)propyl)-isoxazolin-5-(R,S)-ylcarbonyl!-(S)-2,3-diaminopropionic acid:

The product of part F (30 mg, 0.051 mmol) was dissolved in methylene chloride (5 mL) and treated with 0.2 mL trifluoroacetic acid according to the procedure of Ex. 284, Part I, to provide the title product (25 mg, 90%) as a glassy foam: NMR (DMSO-d₆) δ 8.36 (s, 1H), 8.20 (m, 1H), 7.60 (m, 2H), 7.38 (bs, 5H), 7.28 (m, 1H), 5.08 (s, 2H), 4.88 (m, 1H), 4.36 (b, 2H), 3.76 (b, 2H), 3.48-3.08 (9H), 2.30 (b,2H), 1.82 (b, 2H); mass spec (ESI) m/z 475.3 (M+H⁺, 100%).

EXAMPLE 284 2(S)-benzyloxycarbonylamino-3- 2- 3-(2-(N-imidazolin-2-yl)-aminoethyl)isoxazolin-5-(R,S)-yl!ethylcarbonylamino!propionic acid

A. 2-(2-Pthalimidoethyl)-1,3-dioxolane:

To a solution of potassium pthalimide (15.20 g, 82.0 mmol) dissolved in 150 mL dimethylformamide was added 2-(2-Bromoethyl)-1,3-dioxolane (14.86 g, 82.0 mmol). After stirring at room temperature for 22 h, the mixture was diluted with excess water and stirred. The resulting white precipitate was collected and dried (17.0 g, 84%): NMR (CDCl₃) δ 7.84 (m, 2H), 7.72 (m, 2H), 4.98 (t, 1H), 3.99 (m, 2H), 3.86 (m, 4H), 2.10 (m, 2H); mass spec (NH₃ -CI) m/z 248.1 (M+H⁺, 100%).

B. 3-Phthalimidopropionaldehyde:

The product of Ex. 284, part A (17.0 g, 69.0 mmol) was dissolved in dioxane (150 mL) and treated with 1:1 1N HCl/water (200 mL). After stirring at room temperature overnight, the mixture was heated to reflux for 3 h. The reaction was concentrated, neutralized with aqueous NaHCO₃, extracted into chloroform, and dried (Na₂ SO₄). Concentration of the solvent provided the title product (14.0 g, 100%): NMR (CDCl₃) δ 7.82 (m, 2H), 7.78 (m, 2H), 4.02 (t, 2H), 2.88 (t, 2H).

C. 3-Phthalimidopropionaldehyde oxime:

The product of Ex. 284, part B (14.0 g, 69.0 mmol) was reacted with hydroxylamine hydrochloride (5.80 g, 83.0 mmol) in pyridine (200 mL). After stirring overnight, the pyridine was evaporated and the resultant mixture diluted with water. The precipitate was collected and dried providing the title product as a white solid (8.00 g, 53%): NMR (CDCl₃) δ 7.82 (m, 2H), 7.76 (m, 2H), 6.82 (t, 1H), 3.90 (m 4H).

D. tert-Butyl 3-(3- 2-phthalimidoethyl!-isoxazolin-5-(R,S)-yl)-propionate:

The product of Ex. 284, part C (2.69 g, 12.35 mmol) was combined with N-chlorosuccinimide (1.65 g, 12.35 mmol) and pyridine (2 drops) in chloroform (30 mL). After stirring at room temperature for 1 h, t-butyl pentenoate (3.86 g, 24.7 mmol) and triethylamine (2.1 mL, 14.82 mmol) were added and stirring continued at room temperature. After 18 h, the resulting mixture was concentrated and flash chromatographed (7:3 hexane/ethyl acetate) to provide 2.50 g (54%) of the title product: NMR (CDCl₃) δ 7.82 (m, 2H), 7.78 (m, 2H), 4.60 (m, 1H), 3.96 (t, 2H), 3.18 (dd,1H) 2.72 (m, 3H), 2.38 (dt, 2H), 1.84 (q, 2H), 1.42 (s, 9H); mass spec (NH₃ -CI) m/z 373.3 (M+H⁺, 100%).

E. 3-(3- 2-Phthalimidoethyl!-isoxazolin-5-(R,S)-yl)propionic acid:

The product of Ex. 284, part D (500 mg, 1.34 mmol) was dissolved in 10 mL of methylene chloride and 5 mL trifluoroacetic acid. After 4 h the solution was concentrated to provide the title product as a foamy solid (420 mg, 100%): NMR (DMSO-d₆) δ 7.82 (m,2H), 7.76 (m, 2H), 4.62 (m, 1H), 3.96 (t, 2H), 3.20 (m, 1H), 2.78 (m, 3H), 2.56 (m, 2H), 1.96 (q, 2H).

F. tert-Butyl 2(S)-benzyloxycarbonylamino-3- 2- 3-(2-phthalimidoethyl)isoxazolin-5-(R,S)-yl!ethylcarbonylamino!-propionate:

The product of Ex. 284, part E (420 mg, 1.33 mmol) was combined with t-butyl N² -benzyloxycarbonyl-2-(S)-2,3-diaminopropionate (M. Mokotoff and L. Logue, J. Med. Chem., 1981, 24, 554) (390 mg, 1.33 mmol), O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate (430 mg, 1.33 mmol), and triethylamine (0.6 mL, 4.00 mmol) in 25 mL of ethyl acetate. After stirring at room temperature for 20 h, the reaction was concentrated and flash chromatographed (ethyl acetate) to provide 647 mg (86%) of the title product: NMR (CDCl₃) δ 7.82 (m, 2H), 7.72 (m, 2H), 7.36 (bs, 5H), 6.06 (b,1H), 5.80 (b, 1H), 5.08 (bd, 2H), 4.60 (b, 1H), 4.37 (b, 1H), 3.97 (bt, 1H), 3.62 (m, 1H), 3.07 (m, 1H), 2.70 (b, 3H), 2.24 (b, 1H), 1.97 (m, 1H), 1.44 (s, 9H); mass spec (ESI) m/z 593.4 (M+H⁺, 100%).

G. tert-Butyl 2(S)-benzyloxycarbonylamino-3- 2- 3-(2-aminoethyl)isoxazolin-5-(R,S)-yl!ethylcarbonylamino!propionate:

The product of Ex. 284, part F (450 mg, 0.76 mmol) was treated with hydrazine (0.1 mL, 1.90 mmol) in 7 mL of ethanol and stirred at room temperature overnight. The mixture was concentrated and taken up in water, the pH was adjusted to 11 and the resultant extracted with methylene chloride. The organic layer was dried (Na₂ SO₄), filtered, and concentrated providing 250 mg (71%) of the title product as a gummy solid: NMR (CDCl₃) δ 7.40 (m,5H), 6.20 (b, 1H), 5.85 (b, 1H), 5.10 (s, 2H), 4.60 (b, 1H), 4.30 (b, 1H), 3.60 (bt, 2H), 3.00-2.96 (m, 3H), 2.60 (2dd, 1H), 2.42 (b, 2H), 2.30 (b, 2H), 2.00-1.80 (m, 2H), 1.58 (bs, 2H), 1.42 (s, 9H); mass spec (ESI) m/z 463.3 (M+H⁺, 100%).

H. tert-Butyl 2(S)-benzyloxycarbonylamino-3- 2- 3-(2-(N-imidazolin-2-ylamino)ethyl)isoxazolin-5-(R,S)-yl!ethylcarbonylamino!propionate:

The product of Ex, 284, part G (132 mg, 0.290 mmol) was reacted with 2-methylthio-2-imidazoline hydroiodide (84 mg, 0.342 mmol) in 5 mL pyridine over an oil bath heated at 120 C.°. After 18 h the mixture was cooled and concentrated providing the title product (102 mg, 66%): NMR (CDCl₃) δ 8.08 (b, 1H), 7.60 (b, 1H), 7.39 (bs, 5H), 7.20 (b, 1H), 6.18 (b, 1H), 5.82 (b 1H), 5.10 (s, 2H), 4.62 (b, 1H), 4.30 (b, 1H), 3.61 (bs, 2H), 3.58 (m, 2H), 3.02-2.94 (m, 3H), 2.60 (m, 1H), 2.40 (b, 2H), 2.30 (b, 2H), 1.94 (m, 2H), 1.40 (s, 9H); mass spec (ESI) m/z 531.5 (M+H⁺, 100%).

I. 2(S)-benzyloxycarbonylamino-3- 2- 3-(2-(N-imidazolin-2-yl)-aminoethyl)isoxazolin-5-(R,S)-yl!ethylcarbonylamino!propionic acid

The product of Ex. 284, part H (100 mg, 0.188 mmol) was dissolved in 2 mL of methylene chloride and 0.2 mL trifluoroacetic acid. After 5 h, the solution was concentrated and triturated with ether to provide 70.0 mg (64%) of the title product: NMR (DMSO-d₆) δ 8.20 (m, 1H), 8.04 (m, 1H), 7.53 (bd, 1H), 7.40 (bs, 5H), 5.04 (s, 2H), 4.42 (m,1H), 4.08 (m, 1H), 3.52-3.20 (m, 10H), 3.02 (m, 2H), 2.60 (m, 1H), 2.12 (m, 2H), 1.70 (m, 2H); mass spec (ESI) m/z 475.3 (M+H⁺, 100%).

General Procedure for synthesis of 1-(9-fluorenylmethoxycarbonylamino)alkenes

A. 1-(p-Toluensulfonyloxy)-3-butene:

3-Butene -1-ol (10.5 g, 0.146 mol) was dissolved in 75 mL of pyridine and cooled in an ice bath. p-Toluenesulfonyl chloride (28.5 g, 0.150 mol) was added slowly. The solution was stirred for 8 h in an ice bath then allowed to stir at room temperature overnight. The solution was poured into saturated NaHCO₃ and ice. After the ice melted the mixture was extracted with dichloromethane and the organic layer evaporated to provide the title compound (28.6 g, 86%). ¹ H NMR (CDCl₃): δ 2.32-2.44 (m, 2H), 2.45 (s, 3H), 4.05 (t, J=10 Hz, 2H), 5.02-5.12 (m, 2H), 5.60-5.74 (m, 1H), 7.35 (d, J=8 Hz, 2H), 7.78 (d, J=8 Hz, 2H). mass spectrum m/z 311 (M+NH₄, base peak), 294 (M+H).

B. 1-amino-3-butene:

The product of Ex. 637, part A (28.6 g, 0.126 mol) was dissolved in 25 mL of dimethylformamide. Sodium azide (23.5 g, 0.354 mol) was added in several portions and the reaction mixture allowed to stir at room temperature overnight. The reaction mixture was poured into 100 mL of water and 200 mL of diethyl ether and the layers separated. The organic layer was washed with 100 mL of water and 100 mL of brine and dried over magnesium sulfate. The crude azide solution was reacted without further purification. Triphenylphosphine (34.0 g, 0.129 mol) was added and the reaction mixture stirred for 6 h at room temperature. 2.3 mL of water was added to the reaction and the solution was stirred overnight. The diethyl ether layer was distilled and 4.62 g (52%) of the title compound was obtained. ¹ H NMR (CDCl₃): δ 1.60 (br s, 2H), 2.20 (q, J=9 Hz, 2H), 2.78 (t, J=9 Hz, 2H), 5.05-5.15 (m, 2H), 5.70-5.84 (m, 1H).

C. 1-(9-Fluorenylmethoxycarbonylamino)-3-butene:

The product of Ex. 637, part B (5.11 g, 65 mmol) was dissolved in 50 mL of tetrahydrofuran and 50 mL of 10% NaHCO₃ and cooled in an ice bath. 9-Fluorenylmethoxycarbonyl chloride (16.8 9, 65 mmol) was added in several portions, after 4 h the ice bath was removed and the reaction mixture allowed to stir at room temperature overnight. The reaction mixture was poured into 200 ml of water and extracted with diethyl ether. The combined organic layers were evaporated to leave a white solid which was purified by flash column chromatography (hexane:ethyl acetate 3:1) to yield 5.4 g (28%) of the desired product. ¹ H NMR (CDCl₃) δ 2.22-2.36 (m, 2H), 3.22-3.34 (m, 2H), 4.24 (t, J=8 Hz, 1H), 4.40 (d, J=8 Hz, 1H), 4.60 (br s, 1H), 5.06-5.16 (m, 2H), 5.72-5.84 (m, 1H), 7.26-7.44 (m, 4H), 7.58 (d, J=9 Hz, 2H), 7.78 (d, J=9 Hz, 2H). Mass spectrum: m/z 311 (M+NH₄, base peak), 294, (M+H), HRMS Calcd 294.1494 observed 294.1505.

EXAMPLE 583 2(S)-Benzyloxycarbonylamino-3- 5-(4-(N- imidazolin-2-yl!amino)butyl)isoxazolin-3-(R,S)-ylcarbonyl!aminopropionic acid:

A. 1-(9-Fluorenylmethoxycarbonylamino)-5-hexene

The title alkene was prepared in 36% yield according to the method described in the above general procedure, except starting with 5-hexene-1-ol. ¹ H NMR (CDCl₃) δ 1.34-1.58 (m, 4H), 2.02-2.14 (m, 2H), 3.12-3.24 (m, 2H), 4.20 (t, J=8 Hz, 1H), 4.40 (d, J=8 Hz, 2H), 4.72 (s, 1H), 4.90-5.04 (m, 2H), 5.70-5.84 (m, 1H), 7.26-7.42 (m, 4H), 7.58 (d, J=9 Hz, 2H), 7.76 (d, J=9 Hz, 2H).

B. 3-Methoxycarbonyl-5- (9-fluorenylmethoxycarbonylamino)butyl!-Δ² -isoxazoline:

1-(9-Fluorenylmethoxycarbonylamino)-5-hexene (2.00 g, 6.22 mmol) and phenylisocyanate (3.70 g, 31.11 mmol) was dissolved in 40 mL of benzene. Thirty drops of diisopropylethylamine was added followed by methyl nitroacetate (1.48 g, 12.44 mmol) and stirred at room temperature for 48 h. The reaction mixture was filtered and the filtrate evaporated. The residue was purified by flash column chromatography (hexane:ethyl acetate 3:1 to 1:1) to yield 1.83 g (70%) of a tan solid. ¹ H NMR (CDCl₃) δ 1.32-1.84 (m, 6H), 2.78-2.90 (m, 1H), 3.12-3.34 (m, 3H), 3.86 (s, 3H), 4.20 (t, J=7 Hz, 1H), 4.40 (d, J=7 Hz, 2H), 4.72-4.86 (m, 2H), 7.26-7.42 (m, 4H), 7.58 (d, J=9 Hz, 2H), 7.80 (d, J=9 Hz, 2H). mass spectrum m/z 440 (M+NH₄), 423 (M+H), 244 (base peak).

C. 3-Carboxy-5- (9-fluorenylmethoxycarbonylamino)butyl!-Δ.sup. 2-isoxazoline:

The product of Ex. 583, Part B (1.83 g, 4.33 mmol) was dissolved in 50 mL Of tetrahydrofuran and 25 mL of water and cooled in an ice bath. Lithium hydroxide (174 mg, 4.15 mmol) was dissolved in 2 mL of water and added to the tetrahydrofuran/water solution. After approximately 10 min the reaction mixture was quenched with 10% HCl, to pH=3. The mixture was extracted with diethyl ether, dried over magnesium sulfate and evaporated to a syrup. Trituration with benzene:pentane 3:1 and filtration afforded a yellow solid which was recrystalized from benzene chloroform 5:1 to yield 1.18 g (67%) of the title compound as a white powder. ¹ H NMR (CDCl₃) δ 1.34-1.82 (m, 6H), 2.80-2.98 (m, 1H), 3.10-3.32 (m, 3H), 4.16-4.30 (m, 1H), 4.40-4.52 (m, 2H), 4.80-4.90 (m, 2H), 6.50 (br s, 1H), 7.26-7.42 (m, 4H), 7.58 (d, J=9 Hz, 2H), 7.76 (d, J=9 Hz, 2H). Mass spectrum m/z 426 (M+NH₄) 382 (M+NH₄ --CO₂, base peak) HRMS calcd 409.1763 observed 409.1748.

D. 3-tert-Butyloxycarbonyl-5- 4-(9-fluorenylmethoxycarbonylamino)butyl!-.DELTA.² -isoxazoline

The compound of Ex. 583, Part C (715 mg, 1.75 mmol) was dissolved in 2 mL of dichloromethane and cooled in an ice bath. 2 mL of Ca. 3.5M solution of N,N'-diisopropyl-O-t-butyl isourea was added and the reaction mixture stirred for 8 h, and the ice bath removed, and stirred overnight at room temperature. The reaction mixture was cooled in an ice bath and 2 mL of glacial acetic acid was added dropwise, during which time vigorous gas evolution occured. The reaction mixture was diluted with ice water and cautiously neutralized with saturated Na₂ CO₃, and extracted three times with ethyl acetate. The organic layer was dried over MgSO₄, filtered and evaporated. The residue was taken up in 20 mL of 1:1 dichloromethane/ethyl acetate and filtered. the filtrate was evaporated and purified by flash column chromatography, CH₂ Cl₂ :hexane:ethyl acetate, 2:2:1 to yield 375 mg (46%) of the title compound. ¹ H NMR (CDCl₃) δ 1.35-1.78 (m, 15H), 2.80, (dd, J=16, 8 Hz, 1H), 3.15-3.30 (m, 3H), 4.22 (t, J=7 Hz, 1H), 4.40 (d, J=7 Hz, 2H), 4.70-4.80 (m, 2H), 7.28-7.44 (m, 4H), 7.60 (d, J=9 Hz, 2H), 7.78 (d, J=9 Hz, 2H). Mass spectrum m/z 482, (M+NH4), 465, (M+).

E. 3-tert-Butyloxycarbonyl-5-(4-aminobutyl)-Δ² -isoxazoline

The compound of Ex. 583, Part D (375 mg, 0.81 mmol) was dissolved in 20 mL of dichloromethane, 0.5 mL of piperidine was added and the reaction mixture stirred overnight at room temperature. The solvent was evaporated and the residue purified by flash column chromatography CH₂ Cl₂ :isopropanol 2% to CH₂ Cl₂ :isopropanol 2%:triethylamine:0.5% to yield 163 mg (83%) of the title compound. ¹ H NMR (CDCl₃) δ 1.35-1.80 (m, 15 H), 2.40 (br s, 2H), 2.70-2.86 (m, 3H), 3.22 (dd, J=16, 8 Hz, 1H), 4.80 (m, 1H). Mass spectrum m/z 243 (M+H, base peak).

F. 3-tert-Butyloxycarbonyl-5- 4-(imidazolin-2-ylamino)butyl!-Δ² -isoxazoline hydroiodide

The compound of Ex. 583, Part E (163 mg, 0.67 mmol) and 2-methylthioimidazoline (180 mg, 0.73 mmol) was dissolved in pyridine and gently refluxed overnight. The solvent was evaporated and the residue purified by preparatory TLC, chloroform, 20% methanol, to yield 100 mg (33%) of the title compound. ¹ H NMR (CDCl₃) δ 1.35-1.80 (m, 15H), 2.84 (dd, J=16 Hz, 8 Hz, 1H), 3.20-3.32 (m, 3H), 2.56 (br s, 3H), 3.74 (s, 4H), 4.82 (m, 1H).

Mass spectrum m/z 311 (M (-HI)+H).

G. tert-Butyl-2-benzyloxycarbonylamino-3- 5- 4- (N-imidazolin-2-yl)amino!butyl-5(R,S)-isoxazolin-3-yl!carbonylamino!propionate:

The compound of Ex. 583, Part F (100 mg, 0.23 mmol) was suspended in 2 mL of dichloromethane and 2 mL of trifluoroacetic acid was added. The reaction mixture was stirred for 1 h. at room temperature and the solvent evaporated to give the brown oil to which was dissolved in 1 mL of DMF. t-Butyl 3-amino-2-S-(benzyloxycarbonylamino)propionate (67 mg, 0.23 mmol) was added followed by benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (110 mg, 0.24 mmol) and diiosopropylethyl amine (65 mg, 0.50 mmol) and stirred at room temperature overnight. The solvent was evaporated under reduced pressure and the residue purified by preparatory TLC, chloroform, 20% methanol to yield 42 mg, (28%) of the title compound. ¹ H NMR (CDCl₃) δ1.35-1.80 (m, 15H), 2.80-3.20 (m, 4H), 3.70 (s, 4H), 4.24 (t, J=5 Hz, 1H), 4.36 (t, J=5 Hz, 1H), 4.78 (m, 1H), 5.10 (s, 2H), 7.35 (s, 5H).

H. 2(S)-benzyloxycarbonylamino-3- 5-(4-(N- imidazolin-2-yl!amino)butyl) isoxazolin-3-(R,S)-ylcarbonyl!aminopropionic acid:

The product from Ex. 583, Part G was suspended in 2 ml of dichloromethane and 1 mL of trifluoroacetic acid was added. the reaction mixture was stired at room temperature for 1 h. The solvent was evaporated and the residue triturated with diethyl ether to provide the title compound. ¹ H NMR (CDCl₃) δ1.32-1.76 (m, 6H), 2.80-2.90 (m, 1H), 3.16-3.80 (m, 6H), 4.40-4.52 (m, 2H), 4.70-4.82 (m, 1H), 5.04-5.16 (m, 1H), 7.24-7.42 (m, 5H). mass spectrum m/z 475.4

EXAMPLE 637 2(S)-Benzyloxycarbonylamino-3- 5-(3-(N- imidazolin-2-yl!amino)propyl)isoxazolin-3-(R,S)-ylcarbonyl!aminopropionic acid

A. 1-(9-Fluorenylmethoxycarbonylamino)-4-pentene:

The title alkene was prepared in 49% yield according to the methods described in the above general procedure, except starting with 4-pentene-1-ol. ¹ H NMR(CDCl₃) δ 1.58-1.70 (m, 2H), 2.02-2.16 (m, 2H), 4.22 (t, J=8 Hz, 1H), 4.42 (d, 8 Hz, 2H), 4.75 (br s, 1H), 4.94-5.08 (m, 2H), 5.72-5.84 (m, 1H), 7.26-7.42 (m, 4H), 7.58 (d, J=9 Hz, 2H), 7.78 (d, J=9 Hz, 2H). Mass spectrum m/z 325 (M=NH₄, base peak) 308, (M+H). HRMS calcd 308.1650, observed 308.1650.

B. 3-Carboxy-5- (9-fluorenylmethoxycarbonylamino)propyl!-Δ² -isoxazoline:

The title compound was prepared according to Ex. 583, Part B-C in 58% overall yield starting with 1-(9-Fluorenylmethoxy-carbonylamino)-4-pentene and methyl nitroacetate. ¹ H NMR (DMSO) δ 1.30-1.62 (m, 4H), 2.78 (dd J=16, 8 Hz, 1H), 2.98 (d, J=7 Hz, 2H), 3.20 (dd, J=16, 8 Hz, 1H), 4.20 (t, J=7 Hz, 1H), 4.30 (d, J=7 Hz, 2H), 4.68-4.80 (m, 1H, 7.26-7.44, m, 4H), 7.64 (d, J=9 Hz, 2H), 7.84 (d, J=9 Hz, 2H). 13.40 (br s, 1H).

Mass spectrum m/z 395 (M+H), HRMS calcd 395.1606 observed 395. 1591.

EXAMPLE 667 2-(S)-Benzyloxycarbonylamino-3- 5-(R,S)-(4-(N-(pyridin-2-yl)amino)butyl)isoxazolin-3-ylcarbonyl!aminopropionic acid hydrochloride salt

A. 3-Ethoxycarbonyl-5- -4-(hydroxy)butyl!isoxazoline:

5-Hexene-1-ol (5.0 g, 0.05M) was dissolved in 30 mL of tetrahydrofuran, an aqueous solution of NaHCO₃ (29.4 g, 0.35M in 20 mL water) was added and the reaction mixture cooled in an ice bath. Ethyl chlorooximinoacetate (11.4 g, 0.075M) was added over 15 min. in several portions. The reaction mixture was stirred in an ice bath for 6 h. An additional amount of ethyl chlorooximinoacetate (7.75 g, 0.05M) was added and the reaction mixture was allowed to stir overnight, during which time the ice bath melted. The reaction mixture was partitioned between ethyl acetate and water and the organic layer was separated, dried over magnesium sulfate, filtered and evaporated. The crude product was purified by flash column chromatography (hexane/ethyl acetate 3:1) to yield the title compound as a colorless oil (9.22 g, 86%). ¹ H NMR (CDCl₃): δ 1.3 (t, J=7 Hz, 3H), 1.40-1.90 (m, 6H) 2.80-2.94 (m, 1H, 3.20-3.54, m, 1H), 3.66 (br s, 2H, 4.34, q, J=7 Hz, 2H), 4.78-4.90 (m, 1H). mass spectrum m/z 233, (M+NH₄, base peak), 216, (M+) Alternatively the title compound can be prepared by the following procedure.

5-Hexene-1-ol (5 g, 0.05M) and diethyl nitromalonate (15.4 g, 0.075M) was dissolved in mesitylene (50 mL) and refluxed for 5 h. The solvent was removed in vacuo, and the residue purified by flash column chromatography on silica gel (hexane/ethyl acetate 1:1) to provide the title product (5.11 g, 47.5%).

B. 3-Ethoxycarbonyl-5- -4-oxobutyl!isoxazoline:

Oxalyl chloride (7.30 g, 0.0575M) was dissolved in anhydrous methylene chloride and cooled to -60° C. in a dry-ice/CHCl₃ bath. Dimethylsulfoxide (9.38 g, 0.12M) was dissolved in anhydrous methylene chloride and added dropwise over 30 min. to the solution of oxalyl chloride, and allowed to stir for an additional 30 min. The product of Ex. 667, part A. (10.75 g, 0.05M) was dissolved in anhydrous methylene chloride (30 mL) and added to the reaction mixture dropwise over 45 min, and allowed to stirred for an additional 30 min. Triethylamine (25.25 g, 0.25M) was added dropwise over 15 min. The ice bath was removed and the reaction mixture allowed to warm to room temperature. The reaction mixture was diluted with methylene chloride (100 mL) and washed with water, 1N HCl, water, and brine. The organic layer was separated and dried over magnesium sulfate and evaporated to yield the title compound as a colorless oil (9.54 g, 90%). ¹ H NMR (CDCl₃): δ 1.37 (t, J=7 Hz, 3H), 1.60, 1.92 (m, 6H), 2.52 (t J=6 Hz, 2H), 2.80-2.92 (m, 1H, 3.22-3.36, m, 1H), 4.36 (q, J=7 Hz, 2H), 4.74-4.88 (m, 1H, 9.58, s, 1H).

C. 3-Ethoxycarbonyl-5- 4-(-N-(pyridin-2-yl)amino)butyl!isoxazoline

The product of Ex. 667 part B. (9.40 g, 0.044M) was dissolved in dichloroethane (100 mL) and cooled in an ice bath. 2-Aminopyridine (4.57 g, 0.048M) was added followed by the addition of sodium triacetoxyborohydride (14.0 g, 0.066M). The ice bath was removed and the reaction mixture allowed to stir at room temperature for 4 h. The reaction mixture was cautiously poured into a saturated solution of sodium bicarbonate (200 mL), and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium carbonate, filtered and evaporated to yield a semisolid. The crude product was triturated with a mixture of ether and hexane, and the product collected by filtration (8.93 g, 70%) ¹ H NMR (CDCl₃): δ 1.30 (t, J=7 Hz, 3H), 1.40-1.90 (m, 6H, 2.80-2.92, m, 1H), 3.20-3.34 (m, 2H), 4.34 (q, J=7 Hz, 2H), 4.70-4.90 (m, 2H), 6.30 (d, J=9 Hz, 1H), 6.48 (t, J=6 Hz, 1H), 7.42 (t J=6 Hz, 1H), 8.04 (d, J=4 Hz, 1H).

D. 3-Ethoxycarbonyl-5- 4-(N-(pyridin-2-yl)-N-(tert-butyloxycarbonyl)amino)butyl!isoxazoline

The product of Ex. 667 part C. (8.93 g, 0.031M) was dissolved in methylene chloride. 4-Dimethylaminopyridine (374 mg, 0.003M) was added followed by di-tert-butyl dicarbonate (14.73 g, 0.067M). The reaction mixture was allowed to stir at room temperature overnight. The mixture was diluted with water and the organic layer separated, dried over magnesium sulfate, filtered and evaporated. The crude product was purified by flash column chromatography (hexane/ethylacetate, 3:1) to yield the title product (9.7 g, 81%). ¹ H NMR (CDCl₃): δ 1.38 (t, J=7 Hz, 3H), 1.40-1.90 (m, 15H), 2.76-2.86 (m, 1H), 3.18-3.30 (m, 1H), 3.93 (t, J=7 Hz, 2H), 4.32 (q, J=7 Hz, 2H), 4.70-4.82 (m, 1H), 7.01 (t, J=6 Hz, 1H), 7.54-7.86 (m, 2H), 8.36 (d, J=4 Hz, 1H).

E. 5- 4-(N-(Pyridin-2-yl)-N-(tert-butyloxycarbonyl)amino)butyl!isoxazolin-3-carboxylic acid:

The product of Ex 667 part D, (10.7 g, 0.027M) was dissolved in a mixture of 20 mL of tetrahydrofuran and 20 mL of water, and cooled in an ice bath. Lithium hydroxide (1,73 g, 0.41M) was dissolved in 5 ml of water and added to the ester solution. the reaction mixture was stirred for 45 m. TLC of the reaction mixture (hexane/ethyl acetate, 3:1) indicated that no ester remained. 1M Citric acid solution (40 mL) was added and the mixture was extracted several times with ethyl acetate (until TLC of the organic layer showed no product). The combined orgainic layers were dried over magnesium sulfate, filtered, and evaporated and dried under high vacuum to yield the title product as a light yellow semisolid (9.9 g, 99%). ¹ H NMR (CDCl₃): δ 1.24-1.82 (m, 12H), 2.78-2.9 (m, 1H), 3.20-3.32 (m, 1H), 3.90 (t J=7 Hz, 2H), 4.78-4.90 (m, 1H), 7.10 (t J=6 Hz, 1H), 7.52 (d, J=8 Hz, 1H), 7.70 (t, J=6 Hz, 1H), 8.42 (t, J=4 Hz, 1H).

Mass spectrum m/z 364.3 (M+H, base peak)

F. tert-Butyl-2-(S)-benzyloxycarbonylamino-3- 5-(R,S)-(4-(N-(pyridin-2-yl)-N-(tert-butyloxycarbonyl)amino)butylisoxazolin-3-ylcarbonyl!aminopropionate:

tert-Butyl N² -benzyloxycarbonyl-2-(S)-2,3-diaminopropionate (M. Mokotoff and L. Logue, J. Med. Chem., 1981, 24, 554) (2.59 g, 8.806 mmol), and the carboxylic acid from Ex. 667 part E. (3.20 g, 8.806 mmol) were dissolved in N'N'-dimethylformamide (20 mL). N'-methylmorpholine (2.72 g, 26.856 mmol) and benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (4.09 g, 9.246 mmol) were added and the reaction mixture stirred for 48 h at room temperature under nitrogen. Concentration in vacuo to an orange oil which was purified by silica gel flash column chromatography (hexane/ethyl acetate (2:1), to yield the title compound as a pale yellow syrup (4.56 g, 83%). ¹ H NMR (CDCl₃): δ 1.35-1.77 (m, 6H), 1.48 (s, 9H), 1.50 (s, 9H), 2.74-2.83 (d of d, J=17.58, 8.05 Hz, 1H), 3.14-3.24 (d of d of d, J=17.58, 8.05, 1.06 Hz, 1H), 3.68-3.79 (m, 2H), 3.90-3.95 (t, J=6.96 Hz, 2H), 4.35-4.41 (m, 1H), 4.67-4.79 (m, 1H), 5.11 (s, 2H)(, 5.66-5.69 d, J=6.96 Hz, 1H), 6.94-6.97 (t, J=5.36 Hz, 1H), 6.98-7.06 (d of d, J=4.76, 1.84 Hz, 1H), 7.28-7.37 (m, 5H), 7.51-7.59 (t of d, J=6.96, 1.84 Hz, 1H), 7.58-7.67 (t of d, J=6.96, 1.83 Hz, 1H), 8.35-8.39 (d of d, J=4.76, 1.83, 1H). Mass spectrum m/z=640.4 (M+H), 264.2 (base peak).

G. 2-(S)-Benzyloxycarbonylamino-3- 5-(R,S)-(4-(N-(pyridin-2-yl)amino)butyl)isoxazolin-3-ylcarbonyl!aminopropionic acid:

The product of Ex. 667 part F (60 mg, 0.094 mmol) was dissolved in 4N HCl in dioxane (2 mL), and stirred at room temperature for 5 h. under nitrogen. The solvent was evaporated in vacuo and the residue purified by reverse phase (C18) HPLC to yield the title compound (39 mg, 87%). ¹ H NMR (CDCl₃): δ 1.35-1.77 (m, 6H), 2.74-2.83 (m, 2H), 3.20-3.40 (m, 3H), 3.55-3.80 (m, 3H), 4.40 (br s, 1H), 4.55 (br s, 1H), 5.02 (t, J=8 Hz, 2H), 6.83 (br t, 1H), 7.02 (d, 6 Hz, 1H), 7.28 (s, 5H), 7.78 (d, J=4 Hz, 1H), 7.85 (t, J=5 Hz, 1H). Mass spectrum m/z=484.3. (M+H).

EXAMPLE 669 2-(S)-Phenylsulfonylamino-3- 5-(R,S)-(4-(N-(pyridin-2-yl)amino)butyl)isoxazolin-3-ylcarbonyl!aminopropionic acid trifluoroacetate salt

A. Methyl-2-(S)-phenylsulfonylamino-3- 5-(R,S)-(4-(N-(pyridin-2-yl)-N-(tert-butyloxycarbonyl)amino)butylisoxazolin-3-ylcarbonyl!aminopropionate:

Methyl 3-amino-2-phenylsulfonylaminopropionate (Hartman, G. D., Prugh, J. D., Egbertson, M. S., Duggan, M. E. Hoffman, W. PCT Int. Appl WO 9408577 A1 940428) (8.82 g, 24.3 mmol) and the product of Ex 667 part E, (7.15 g, 24.257 mmol) was disolved in N'N'-dimethylformamide (100 ml). N'-Methylmorpholine (7.61 g, 75.197 mmol) and Benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (12.88 g, 29.108 mmol) were added and the reaction mixture stirred for 15 h. at room temperature under a nitrogen atmosphere. The solvent was removed in vacuo to provide the crude product as an orange syrup which was purified by silica gel flash chromatography (hexane/ethyl acetate, 1:1), to yield the title compound as a light yellow oil (7.31 g, 57%). ¹ H NMR (CDCl₃): δ 1.34-1.77 (m, 6H), 1.50 (s, 9H), 2.59-2.68 (d of d, J=22.34, 9.52 Hz, 1H), 2.71-2.83 (d of d of d, J=17.58, 8.42, 2.20 Hz, 1H), 2.88-2.96 (d, J=22.34 Hz, 1H), 2.88-3.25 (d of d of d, J=17.58, 10.62, 3.66 Hz, 1H), 3.59 (s, 3H), 3.62-3.69 (m, 2H), 3.93-3.98 (t, J=7.33 Hz, 2H), 4.06-4.12 (m, 1H), 4.70-4.75 (c, 1H), 5.72-5.75 (d of d, J=7.69, 3.36 Hz, 1H), 7.03-7.07 (d of d and c, J=4.76, 1.84 Hz, 2H), 7.47-7.50 (t, J=8.43 Hz, 3H), 7.52-7.65 (t, J=9.15 Hz, 2H), 7.60-7.70, (d of d, J=3.55, 1.83 Hz, 1H), 7.84-7.86 (d of d, J=6.92, 1.46 Hz, 2H), 8.39-8.41 (d, J=4.76 Hz, 1H). Mass spectrum m/z=604.3 (M+H, base peak).

B. 2-(S)-Phenylsulfonylamino-3- 5-(R,S)-(4-(N-(pyridin-2-yl)N-(tert-butyloxycarbonyl)amino)butylisoxazolin-3-ylcarbonyl!aminopropionic acid:

Lithium hydroxide (0.71 g, 16.952 mmol) dissolved in water (10 ml). In a separate flask the product of ex 669 part A, (7.31 g, 12.109 mmol) was dissolved in a mixture of methyl alcohol (200 mL), water (10 mL). The lithium hydroxide solution was added and the reaction mixture was stirred at room temperature for 72 hrs. The resulting red solution was concentrated in vacuo and partioned between ethyl acetate (100 mL) and water (50 mL). A mixture of 1M Hydrochloric Acid (17 ml) in Citric Acid (100 ml) was added until the pH of the aqeous layer was ca. 4. The organic layer was separated and the aqueous layer extracted with ethyl Acetate (2×30 ml). The combined orgainc layers were dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo to provide the title compound as a light yellow oil (6.50 g, 91%). ¹ H NMR (CDCl₃): δ 1.34-1.77 (m, 6H), 1.50 (s, 9H), 2.59-2.68 (d of d, J=22.34, 9.52 Hz, 1H), 2.71-2.83 (d of d of d, J=17.58, 8.42, 2.20 Hz, 1H), 2.88-2.96 (d, J=22.34 Hz, 1H), 2.88-3.25 (d of d of d, J=17.58, 10.62, 3.66 Hz, 1H), 3.59 (s, 3H), 3.62-3.69 (m, 2H), 3.93-3.98 (t, J=7.33 Hz, 2H), 4.06-4.12 (c, 1H), 4.70-4.75 (c, 1H), 5.80-5.86 (d of d, J=7.69, 3.36 Hz, 1H), 6.12-6.15 (d, J=8.06 Hz, 1H), 7.03-7.07 (d of d and c, J=4.76, 1.84 Hz, 2H), 7.16-7.19 (d of d, J=6.92, 1.46 Hz, 2H), 7.24-7.28 (t, J=8.43 Hz, 3H), 7.38-7.57 (t and d of d, J=9.15, 4.02, 2.93 Hz, 2H), 7.64-7.70 (c, 1H), 7.83-7.89 (t, J=6.95 Hz, 1H), 8.39-8.41 (d, J=4.76 Hz, 1H). Mass spectrum m/z=590.2 (M+H, base peak).

C. 2-(S)-Phenylsulfonylamino-3- 5-(R,S)-(4-(N-(pyridin-2-yl)amino)butylisoxazolin-3-ylcarbonyl!aminopropionic acid:

Trifluoroacetic acid (10 ml) was added to the product of Ex 669 part B, (6.50 g, 11.023 mmol) and the reaction mixture was stirred for 3 h at room temperature under nitrogen. The solution was concentrated in vacuo then co-concentrated with toluene (3×100 mL). The resulting oil was purified by gradient reverse phase HPLC (Water/Acetonitrile) to yield the title compound as a white powder (4.78 g, 72% yield, 97.7% purity).

¹ H NMR (CD₃ OD): δ1.34-1.77 (m, 6H), 1.50 (s, 9H), 2.59-2.68 (d of d, J=22.34, 9.52 Hz, 1H), 2.71-2.83 (d of d of d, J=17.58, 8.42, 2.20 Hz, 1H), 2.88-2.96 (d, J=22.34 Hz, 1H), 2.88-3.25 (d of d of d, J=17.58, 10.62, 3.66 Hz, 1H), 3.30-3.36 (t, J=7.33 Hz, 2H), 3.62-3.69 (m, 2H), 4.06-4.12 (c, 1H), 4.70-4.75 (c, 1H), 5.80-5.86 (d of d, J=7.69, 3.36 Hz, 1H), 6.79-6.85 (d, J=4.76 Hz, 1H), 7.00-7.03 (d of d, J=9.16, 2.56 Hz, 1H), 7.46-7.51 (t, J=7.69 Hz, 2H), 7.57-7.59 (t, J=7.33 Hz, 1H), 7.76-7.87 (d, J=6.96, 4H). Mass spectrum m/z=490.2 (M+H, base peak). High resolution mass spectrum m/z 490.176031.

EXAMPLE 695 2(S)-Benzyloxycarbonylamino!-3- 5- (6-aminopyridin-2-yl)propyl!isoxazolin-3-yl!carbonylaminopropionic acid, trifluoroacetate salt

A. tert-Butyl- 2(S)-Benzyloxycarbonylamino!-3- 5- 6-(2,5-dimethylpyrrolyl)pyridin-2-yl!propyl!isoxazolin-3-yl!carbonylaminopropionate:

The product of Ex. 697, Part D (0.43 g, 1.30 mmol) was dissolved in N,N-dimethylformamide (10 mL). (S)-t-Butyl-3-amino-2-benyzloxycarbonylamino-propionate (0.42 g, 1.43 mmol), triethylamine (0.29 g, 2.86 mmol) and O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate (0.46 g, 1.43 mmol), according to the procedure of Ex 284, Part F, to provide the title product (0.33 g, 42%). ¹ HNMR (CDCl₃) δ 1.46 (s, 9H), 1.86 (m, 4H), 2.12 (s, 6H), 2.87 (m, 3H), 3.22 (m, 1H), 3.74 (br s, 2H), 4.38 (m, 1H), 4.78 (m, 1H), 5.11 (s, 2H), 5.68, (bs, 1H), 5.89 (s, 2H), 6.97 (bs, 1H), 7.04 (d, 1H), 7.14 (d, 1H), 7.35 (m, 5H), 7.73 (t, 1H). Mass spectrum: (ESI) m/z 604 (M+H)⁺.

B. 2(S)-Benzyloxycarbonylamino!-3- 5- (6-aminopyridin-2-yl)propyl!isoxazolin-3-yl!carbonylaminopropionic acid, trifluoroacetate salt:

The compound of Ex. 695, Part A (0.33 g, 0.54 mmol), hydroxylamine hydrochloride (0.75 g, 10.8 mmol, and triethylamine (0.55 g, 5.42 mmol) are dissolved in a 4:1 mixture of isopropanol/water (10.0 mL) and refluxed. After 3.5 h, additional hydroxylamine hydrochloride (0.37 g, 5.40 mmol) and triethylamine (0.27 g, 2.71 mmol) are added, and the reaction mixture refluxed for an additional 4 h. The reaction mixture was cooled and sodium carbonate (0.86 g, 8.13 mol) was added. The reaction mixture was stirred for 16 h, then filtered, and the filtrate concentrated. The crude amine was dissolved in a mixture of methylene chloride (4.0 mL) and trifluoroacetic acid (1.0 mL), and stirred for 16 h. The reaction mixture was concentrated to give a thick yellow oil, which was partitioned between ethyl acetate and water. The organic layer was separated and dried over anhydrous sodium sulfate, filtered and concentrated to give a yellow oil. The crude product was purified by preparative reverse phase HPLC using a gradient, 90:10 to 10:90, water/acetonitrile (0.05% trifluoroacetic acid) as eluent, gave the desired product as a trifluoroacetate salt, 15 mg (5%). ¹ HNMR (CDCl₃) δ 1.70 (m, 4H), 2.75 (m, 3H), 3.20 (m, 1H), 3.60 (m, 2H), 4.30 (m, 1H), 4.75 (m, 1H), 5.05 (s, 2H), 6.02 (bs, 1H), 6.59 (d, J=8 Hz, 1H), 6.71 (d, J=8 Hz, 1H), 7.35 (m, 5H), 7.68 (t, J=8 Hz, 1H). Mass spectrum: (ESI) m/z 470(M+H)⁺.

EXAMPLE 697 2-Phenylsulfonylammino!-3- 5- (6-aminopyridin-2-yl)propy1!isoxazolin-3-yl!carbonylaminopropionic acid, trifluoroacetate salt

A. 2-(2,5-Dimethyl-1H-pyrrol-1-yl)-6-methylpyridine:

2-Amino-6-methylpyridine (56.4 g, 0.52 mol), 2,5-hexanedione (59.3 g, 0.52 mol) and acetic acid (5.0 mL) were refluxed in toluene (150 mL), under a Dean-Stark trap for 16 h. The mixture was cooled, an additional portion of 2,5-hexanedione (34.0 g, 0.30 mol) was added and reflux resumed for 7 h. The reaction mixture was cooled, and the solvent was evaporated and the residue was disolved in EtOAc and cautiously washed with saturated NaHCO₃, and then brine. The organic layer was dried with anhydrous sodium sulfate, filtered and concentrated. The residue was flash column chromotragraphy (silica gel, hexane/ethyl acetate, 85:15) to provide 37.5 g (39%) of the title product.

¹ H NMR (CDCl₃) δ 2.12 (s, 6H), 2.59 (s, 3H), 5.88 (s, 2H), 7.02 (d, J=8 Hz, 1H), 7.15 (d, J=8 Hz, 1H).

Mass spectrum: (ESI) m/z 187(M+H)⁺.

B. 2-(2,5-dimethyl-1H-pyrrol-yl)-6-(4-pentenyl)pyridine:

The product of Ex 697 part A, (5.0 g, 0.027 mol) was dissolved in anhydrous tetrahydrofuran (45 mL) and cooled to -78° C. A solution of lithium diisopropylamide (0.032 mol) in anhydrous tetrahydrofuran (50 mL) was precooled to 0° C., and added to the reaction mixture. After stirring for 1.5 h at -78° C., 4-bromo-2-butene (3.78 g, 0.028 mol) was added. This mixture was stirred for an additional 0.5 h, and then allowed to warm to ambient temperature. Saturated ammonium chloride (150 mL) was added, the tetrahydrofuran was evaporated, and the aqueous solution extracted with ethyl acetate (150 mL). The combined organic layers were washed with water (150 mL) and brine (100 mL), then dried over sodium sulfate, filtered and concentrated to yield 5.58 g (86%) of the desired product. ¹ H NMR (CDCl₃) δ 1.87 (m, 2H), 2.10 (t, J=7.3 Hz, 2H), 2.13 (s, 6H), 2.83 (t, J=7.3 Hz, 2H), 4.99 (m, 2H), 5.83 (m, 1H), 5.89 (s, 2H), 7.02 (d, J=7.7 Hz, 1H), 7.13 (d, J=7.7 Hz, 1H), 7.70 (t, J=7.7 Hz, 1H). Mass spectrum: (ESI) m/z 241(M+H)⁺.

C. 5-Ethyl 6- (2,5-dimethylpyrrolyl)pyridin-2-yl!propyl!isoxazolin-3-yl!carboxylate:

The product of ex 697 part B, (2.4 g, 9.98 mmol) was dissolved in a 2:1 mixture of tetrahydrofuran and water (90 mL). Sodium bicarbonate (5.01 g, 59.6 mmol) and ethyl chlorooximidoacetate (1.5 g, 9.98 mmol), according to the procedure of Ex 667, Part A, to provide the title product (1.01 g, 29%). ¹ H NMR (CDCl₃) δ 1.36 (t, 3H), 1.67 (m, 2H), 1.88 (m,2H), 2.12 (s, 6H), 2.85 (m, 3H), 3.25 (m, 1H), 4.33 (q, 2H), 4.84 (m, 1H), 5.89 (s, 2H), 7.04 (d, 1H), 7.14 (d, 2H), 7.73 (t, 1H).

D. 6- (2,5-Dimethylpyrrolyl)pyridin-2-yl!propyl!isoxazolin-3-yl!carboxylicacid:

The product of Ex 697 part C, (1.01 g, 2.84 mmol) was hydrolyzed according to the procedure of Ex 667, Part E, to provide the title product (0.86 g, 92%). ¹ H NMR (DMSO) δ 1.61 (m, 2H), 1.76 (m, 2H), 2.04 (s, 6H), 2.79 (m, 3H), 3.22 (m, 1H), 4.77 (m, 1H), 5.78 (s, 1H), 7.20 (d, 1H), 7.30 (d, 1H), 7.88 (t, 1H).

Mass spectrum: (ESI) m/z 328 (M+H)⁺.

E. Methyl- 2(S)-phenylsulfonylamino!-3- 5- 6-(2,5-dimethylpyrrolyl)pyidin-2-yl!propyl!isoxazolin-3-yl!carbonylaminopropionate:

The product of Ex. 697, Part D (0.43 g, 1.30 mmol) was dissolved in N,N-dimethyl formamide (10 mL), (S)-methyl-3-amino-2-phenylsulfonylaminopropionate (0.42 g, 1.43 mmol), triethylamine (0.29 g, 2.86 mmol) and O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate (0.46 g, 1.43 mmol), were added according to the procedure of Ex 284, Part F, to provide the title product (0.23 g, 31%). ¹ H NMR (CDCl₃) δ 1.85 (m, 4H), 2.13 (s, 6H), 2.79 (m, 1H), 2.88 (t, 2H), 3.23 (m, 1H), 3.67 (m, 1H), 4.11 (m, 1H), 4.79 (m, 1H), 5.76 (m, 1H), 5.89 (s, 2H), 7.02 (bs, 1H), 7.04 (d, 1H), 7.15 (d, 1H), 7.53 (m, 3H), 7.73 (t, 1H), 7.84 (d, 2H). Mass spectrum: (ESI) m/z 568(M+H)⁺.

F. 2(S)-Phenylsulfonylamino!-3- 5- (6-aminopyridin-2-yl)propyl!isoxazolin-3-yl!carbonylaminopropionic acid, trifluoroacetate salt:

The product of Ex, 697, Part E, (0.16 g, 0.29 mmol), hydroxylamine hydrochloride (0.40 g, 5.81 mmol), and triethylamine (0.29 g, 2.91 mmol) were dissolved in a 4:1 mixture of isopropanol/water (10.0 mL) and refluxed. After 3.5 h, additional hydroxylamine hydrochloride (0.37 g, 5.40 mmol) and triethylamine (0.27 g, 2.71 mmol) were added, and the reaction mixture refluxed for an additional 4 h. The reaction mixture was cooled and sodium carbonate (0.46 g, 4.36 mol) was added, the mixture was stirred 16 h. The reaction mixture was filtered and concentrated. The crude amine was taken up in a 4:1 mixture of MeOH/water (10.0 mL) and LiOH.H₂ O (0.012 g, 0.29 mmol) was added. The reaction mixture was stirred 16 h. The methanol was evaporated, and the crude carboxylic acid was dissolved in water and washed with EtOAc. The aqueous phase was adjusted to pH=4.5 with 1M HCl, and the solution absorbed on a pad of C₁₉ reverse phase gel. The pad was washed well with H₂ O and eluted with CH₃ CN. The CH₃ CN eluent was concentrated to give an oily solid. Purification by preparative reverse phase HPLC using a gradient 90:10 water/acetonitrile to 10:90, water/acetonitrile (0.05% trifluoroacetic acid) as eluent, gave the desired product as a TFA salt, 13 mg (8%). ¹ HNMR (CDCl₃) δ 1.80 (m, 4H), 2.81 (m,3H), 3.21 (m, 1H), 3.60 (m, 2H), 4.15 (br s, 1H), 4.80 (br s, 1H), 6.75 (d, J=4.5 Hz, 1H), 6.85 (d, J=8.0 Hz, 1H), 7.56 (m, 4H), 7.82 (m, 3H). Mass spectrum: (ESI) m/z 476(M+H)⁺.

EXAMPLE 849 2- (S)-((2,4,6-trimethylphenyl)sulfonyl)amino!-3- 5-(R,S)-(4-(N-(pyridin-2-yl)amino)butylisoxazolin-3-ylcarbonyl!aminopropionic acid

A. 2-(S)-amino-3- 5-(R,S)-(4-(N-(pyridin-2-yl)-N-(tert-butyloxycarbonyl)amino)butylisoxazolin-3-ylcarbonyl!aminopropionic acid tert-butyl ester:

To the product of example 667 part F, (1.5 g, 2.408 mmol), in methyl alcohol (50 mL) was added Palladium on Barium Sulfate unreduced (0.300 g, 0.482 mmol). The reaction mixture was exposed to hydrogen gas (41 p.s.i.) at room temperature for 15 hours. The reaction mixture was filtered through a celite pad and concentration in vacuo to afforded a light yellow syrup (1.22 g, quantitative yield). ¹ H NMR (CDCl₃): δ 1.34-1.76 (m, 6H), 1.46 (s, 9H), 1.48 (s, 9H), 2.29-2.48 (br s, 2H), 2.78-2.87 (d of d,J=17.58, 8.05 Hz, 1H), 3.19-3.28 (d of d of d, J=17.58, 8.05, 1.06 Hz, 1H), 3.59-3.66 (m, 2H), 3.78-3.81 (m, 1H), 3.86-3.91 (t, J=6.96 Hz, 2H), 4.69-4.78 (m, 1H), 6.98-7.02 (d of d, J=4.76, 1.84 Hz, 1H), 7 12-7.14 (t, J=5.36 Hz, 1H), 7.51-7.56 (t of d, J=6.96, 1.84 Hz, 1H), 7.58-7.64 (t of d, J=6.96, 1.83 Hz, 1H), 8.36-8.38 (d of d, J=4.76, 1.83 Hz, 1H). Mass Spectrum m/z=506.4 (M+H), 197.7 (base peak).

B. 2- (S)-((2,4,6-trimethylphenyl)sulfonyl)amino!-3- 5-(R,S)-(4-(N-(pyridin-2-yl)amino)butylisoxazolin-3-ylcarbonyl!aminopropionic acid:

The product of example 849 part A, (50 mg, 0.0949 mmol), and pyridine (202 mg, 2.585 mmol) were dissolved in dichloromethane (5 mL). 2,4,6-trimethylbenzenesulfonyl chloride (26 mg, 0.119 mmol) was added and the reaction mixture was stirred at room temperature under nitrogen for 8 h. Saturated aqueous sodium bicarbonate (5 mL) was added and the organic layer was separated, dried over anhydrous sodium carbonate and concentrated in vacuo to a syrup. The product was treated with trifluoroacetic acid (5 ml) at room temperature and stirred for 1 hour. The reaction mixture was concentrated in vacuo to a syrup. Toluene (10 mL) was added and the mixture concentrated in vacuo again. The resulting syrup was submitted to gradient HPLC (Water/Acetonitrile) The fractions containing the product were concentrated in vacuo and placed on a lyophilization apparatus overnight, to afford the title compound as a white powder (27 mg, 42% over two steps). ¹ H NMR (CD₃ OD): δ 1.49-1.79 (m, 6H), 2.58 (s, 9H), 2.74-2.82 (d of d, J=17.58, 8.05 Hz, 1H), 3.07-3.16 (d of d of d, J=17.58, 8.05, 1.06 Hz, 1H), 3.31-3.36 (t, J=6.96 Hz, 2H), 3.31-3.65 (d of d, J=13.55, 5.12 Hz, 2H), 4.00-4.06 (m, 1H), 4.74-4.82 (m, 1H), 6.78-6.85 (d of d, J=5.86, 0.73 Hz, 1H), 6.94 (s, 2H), 6.98-7.03 (d of d, J=4.40, 0.05 Hz, 1H), 7 75-7.78 (t, J=5.86 Hz, 1H), 7.81-7.86 (t, J=4.40 Hz, 1H). Mass spectrum m/z=532.2 (M+H , base peak).

EXAMPLE 951 3-{5- 4-(imidazol-2-ylamino)butyl!isoxazoline-3-carbonyl}amino-2S-(2,4,6-trimethylbenzenesulfonylamino)propionic acid trifluoroacetate salt

A. 2-Phthalamidoimidazole:

2-Aminoimidazole sulfate (2.64 g, 20 mmol) was dissolved in 200 mL of anhydrous methanol and cooled to -78° C. A 25% solution of sodium methoxide in methanol (4.57 mL, 20 mmol) was added dropwise. The reaction mixture was allowed to warm to room temperature and stirred for an additional 3 hours. The solution was filtered and concentrated on the rotary evaporator to a brown oil (1.6 g, 96.4%). ¹ H NMR (DMSO) δ 5.0 br.s, 2H, 6.32, s, 2H.

Phthalic anhydride (4.14 g, 29.2 mmol) and 2-aminoimidazole (2.32 g, 29.2 mmol) were heated to 170° C. for 15 min. The crude reaction mixture was purified by flash chromatography (gradient chloroform:methanol 95:5-80:20) to yield 4.66 g (75%) of a brown solid. ¹ H NMR (DMSO) δ 7.16 (br.s, 2H), 7.94-8.06 (m, 4H), 12.35 (br s, 1H). Mass spectrum ESI (M+H)⁺ 214.2

B. 1-Triphenylmethyl-2-phthalamidoimidazole:

The product of Ex. 949, Part A, (4.66 g, 21.9 mmol) was dissolved in 100 mL of anhydrous pyridine and triphenylmethylchloride (9.15 g, 32.82 mmol) was added. The reaction mixture was refluxed for 24 hrs. Pyridine was removed and the residue was purified by flash column chromatography (chloroform:methanol 5-10%) to yield the desired product (2.74 g, 27.5% yield). ¹ H NMR (CDCl₃) δ 6.80 (d, J=1.1 Hz, 1H), 7.06 (t, J=7.3 Hz, 3H), 7.17 (t, J=7.7 Hz, 7H), 7.28 (d, 6H, 7.64, s 4H). Mass spectrum NH₃ -DCI (M+H)⁺ 456.

C. 1-Triphenylmethyl-2-aminoimidazole:

The product of Ex. 949, Part B, (2.60 g, 5.7 mmol) and hydrazine (1.83 g, 57 mmol) were refluxed in 250 mL of anhydrous ethanol for 1 hr. The reaction mixture was cooled and the solvent removed in vacuo. the solid residue was purified by flash column chromatography (chloroform:methanol 10:1) to yield 1.8 g (97%) of a yellow solid. ¹ H NMR (DMSO) δ 6.26 (d, J=1.8 Hz, 1H), 6.51 (d, J=1.8 Hz, 1H), 7.13 (d, J=7 Hz, 6H), 7.33-7.44 (m, 9H). Mass spectrum NH₃ -DCI (M+H), 326.

D. 3-Ethoxycarbonyl-5- 4-(1-triphenylmethylimidazol-2-ylamino)butyl!isoxazoline:

1-Triphenylmethyl-2-aminoimidazole (1.43 g, 4.4 mmol), the product of Ex. 667, Part B, (1.034 g, 4.85 mmol) and magnesium sulfate (2.33 g, 19.4 mmol) were stirred in 250 mL of carbon tetrachloride at room temperature. Progress of the reaction was monitored by NMR. After 90 hrs magnesium sulfate was filtered off and triacetoxyborohydride (3.74 g, 17.65 mmol) was added. The reaction mixture was stirred for an additional 48 hrs. Water (100 mL) was added, the organic layer was separated and the water layer was extracted with ethyl acetate. The combined organic layers were concentrated and purified by flash chromatography (ethyl acetate/hexane 1:1, then ethyl acetate, then ethyl acetate:methanol 20:1) to yield the product as a colorless oil (1.7 g, 74%). ¹ H NMR (DMSO) δ 0.84-0.92 (m, 2H), 1.0 (m, 2H), 1.26 (t, J=7.3 Hz, 3H), 1.31-1.48 (m, 2H), 2.70 (dd, J1=17.6 Hz, J2 =8.4 Hz, 1H), 2.90 (q, J=2.3 Hz, 2H), 3.07 (br. s, 1H), 3.20 (dd, J1=11 Hz, J2=17.6 Hz, 1H), 4.25 (q, J=7.3 Hz, 2H), 4.6 (m, 1H), 6.26 (d, J=1.5 Hz, 1H), 7.50 (d, J=1.5 Hz, 1H), 7.09 (m, 6H), 7.33-7.44 (m, 6H). Mass spectrum: NH3-DCI (M+H)⁺, 523.

E. 5- 4-(1-triphenylmethylimidazol-2-ylamino)butyl!isoxazoline-3-carboxylic acid

The product of Ex. 949, Part D (246 mg, 0.47 mmol) was dissolved in of tetrahydrofuran (2 mL). A 0.5N solution of lithium hydroxide (0.94 mL. 0.47 mmol) was added. The reaction mixture was stirred for 1 h, then aqeous 1N HCl (0.47 mL. 0.47 mmol) was added and the solvent was evaporated. The crude product was purified by flash column chromatography (chloroform/methanol 10:1) to yield the product as a white solid (230 mg, 99%). ¹ H NMR (DMSO) δ 0.84-0.1.31 (m, 6H), 2.57 (dd, J₁ =17.6 Hz, J₂ =8.4 Hz, 1H), 2.89 (q, J=6.6 Hz, 1H), 3.07 (dd, J₁ =17.6 Hz, J₂ =10.6 Hz, 1H), 4.0-4.15 (br.s, 1H), 4.36 (m, 1H), 6.26 (d, J=1.8 Hz, 1H), 6.52 (d, J=1.6 Hz, 1H), 7.10 (d, 6H), 7.34-7.44 (m, 9H). Mass spectrum NH₃ -DCI (M+H)⁺ --CO₂ H, 451.

G. N-(2,4,6 trimethylphenyl)sulfonyl-L-asparagine:

L-Asparagine (20.0 g, 0.15M) was suspended in a mixture of tetrahydrofuran (130 mL) and water (250 mL). Triethylamine (49 g, 0.48M) was added followed by mesitylenesulfonyl chloride (49.7 g, 0.227M), The reaction mixture became slightly exothermic and the solids dissolved over a period of 0.5 h. to yield a yellow solution. The reaction mixture was stirred for 3 h at room temperature, then washed with ether, and methylene chloride. The aqueous layer was separated, and acidified to ca. pH=1.5 with conc. HCl, during which time a thick precipitate formed. After 0.5 h. the product was filtered,washed with water and dried to yield a white solid (34 g, 72%). m.p.=193.5°-195° C. ¹ H NMR (DMSO) δ 2.24 (s, 3H), 2.28 (dd, 1H), 2.45 (dd, 1H), 2.55 (s, 6H), 3.98 (m, 1H), 6.88 (br s, 1H), 6.99 (s, 2H), 7.32 (br s, 1H), 7.82 (d, 2H), 12.58 (br s, 1H). Mass spectrum ESI m/z=315.2, (M+H base peak).

H. 3-Amino-2-(S)-N-(2,4,6 trimethylphenyl)sulfonylaminopropionic acid:

Sodium hydroxide (32 g, 0.80 M), was dissolved in water (200 mL) and cooled in an ice bath. Bromine (19.2 g, 0.12M) was added dropwise over 5 min. and the mixture allowed to stir for 15 min. The product of Ex. 949, Part G, (31.44 g, 0.10M), was added in several portions over a period of ca. 10 min. during which time the yellow color faded. The reaction mixture was gently heated on a steam bath during which time the internal temperature rose to ca. 85° C. After 1 h, the reaction mixture was allowed to cool to room temperature then cooled in an ice bath. The reaction mixture was cautiously acidified to pH=6 with conc. HCl, during which time a solid formed and gas was evolved. The solid was filtered, washed with cold water, and allowed to dry overnight, to yield the product as a white solid (23.9 g, 83%). ¹ H NMR (DMSO) δ 2.26 (s, 3H), 2.59 (s, 6H), 2.80 (dd, 1H), 2.94 (dd, 1H), 3.07 (dd, 1H), 7.06 (s, 2H). Mass spectrum ESI m/z 287.2 (M+H, base peak).

I. tert-Butyl-3-Amino-2-(S)-N-(2,4,6-trimethylphenyl)sulfonylaminopropionate:

The product of Ex. 949, Part H, (11.45 g, 0.04M), was placed in a Parr bottle, and dissolved in dioxane (170 mL), and conc. sulfuric acid (11 mL) was added. The reaction mixture was cooled in a dry ice/acetone bath and ca. 185 ml of isobutylene was added. The bottle was sealed and agitated for 114 h. The bottle was de-pressurized then purged with nitrogen for a brief time. The reaction mixture was poured into a rapidly stirred mixture of water (225 mL) containing sodium hydroxide (17 g) and ether (600 mL) which had been pre-cooled in an ice bath. The layers were separated. The aqueous layer was extracted with additional ether. The pH of the aqueous layer was carefully adjusted with conc. HCl to pH=11 and extracted four times with ether. The organic layers from the pH 11 adjusted extraction were combined, dried with anhydrous sodium sulfate, filtered and evaporated to yield the product as a viscous oil which solidified (8.64 g, 63%).

¹ H NMR (CDCl₃) δ 1.28 (s, 9H), 2.28 (s, 3H), 2.67 (s, 6H), 2.93 (m, 2H), 3.69 (m, 1H), 6.95 (s, 2H).

J. tert-Butyl 3-{5- 4-(1-triphenylmethylimidazol-2-ylamino)butyl!isoxazoline-3-carbonyl}amino-2-(S)-(2,4,6-trimethylbenzenesulfonylamino)propionate:

The product of Ex. 949, Part E, (98 mg, 0.198 mmol) was dissolved in N,N-dimethylformamide (2 mL). The product of Ex 949, Part I, (68 mg, 0.198 mmol), O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate (76 mg, 0.24 mmol) and triethylamine (69 mL, 0.495 mmol) were added and the reaction mixture was stirred at room temperature for 1.5 hrs. The solvent was evaporated and residue was purified by flash chromatography (chloroform/methanol 10:1) to yield the product as a white solid (135 mg, 83%). (NMR***) Mass spectrum (M+H)⁺ 819.4.

K. 3-{5- 4-(1-Triphenylmethylimidazol-2-ylamino)butyl!isoxazoline-3-carbonyl}amino-2-(S)-(2,4,6-trimethylbenzenesulfonylamino)propionic acid:

The product of Ex. 949, Part J, (130 mg, 0.16 mmol) was dissolved in a 1:1 mixture of trifluoroacetic acid and methylene chloride and stirred at room temperature for 5 hrs. The solvent was evaporated and crude product was purified on reverse phase HPLC (C18) to provide the desired product (75 mg, 73%). ¹ H NMR (acetone) δ 0.99-1.48, m, 6H, 2.27, s, 3H, 2.62, s, 6H, 2.67, m, 1H, 3.04-3.21, m, 1H, 3.31,q, J=6.6 Hz, 3.52-3.74, m, 1H, 4.14, m 1H, 4.60, m, 1H, 5.25, br.s, 1H, 6.70, d, J=2.6 Hz, 6.85, d, 1H, 6.98, s, 2H, 7.14, d, J=2.6 Hz, 7.33, m, 6H, 7.48, m, 9H, 7.68, q, 1H; mass spectrum, NH₃ -DCI, 763.3, HRMS calc: 763.329094, found: 763.327781.

L. 3-{5- 4-(imidazol-2-ylamino)butyl!isoxazoline-3-carbonyl}amino-2S-(2,4,6-trimethylbenzenesulfonylamino)propionic acid trifluoroacetate salt:

The product of Ex. 949, Part K, (20 mg, 27 μmol) was dissolved in trifluoroacetic acid (2 mL). Water (0.01 mL) was added and the reaction mixture was refluxed for 1 h. The trifluoroacetic acid was evaporated and the crude reaction product was purified on reverse phase HPLC (C18) to yield the desired prodcut as a white solid (10 mg, 58%). ¹ H NMR 1.34-1.66, m 6H, 2.24, s, 3H, 2.53, s 6H, 2.67-2.76, m, 1H, 3.06-3.14, m 1H, 3.20, m, 2H, 3.30-3.48, m, 2H, 3.91, q, 1H, 4.70, m, 1H, 6.50, br,1H, 6.95, s, 2H, 6.95, s, 2H, 7.94, m, 2H, 8.23, m, 1H, 11.9, s, 2H, 12.5-12.8, br., 1H; Mass spectrum, ESI, (M+H)⁺ 521.4, HRMS; calc. 521.219050, found 521.21823.

EXAMPLE 999j1 2- (S)-((2,4,6-trimethylphenyl)sulfonyl)amino!-3- 5-(R,S)-(4-(N-(3,4,5,6-tetrahydropyridin-2-yl)amino)butylisoxazolin-3-ylcarbonyl!aminopropionic acid

The product of example 849, part B (12 mg, 0.019 mM) was disolved in 50 mL of 1:1 ethyl alcohol and 2-propanol. 5% Palladium on barium sulfate (25 mg) was added and the reaction hydrogenated at 42 psi, at room temperature for 15 h. The reaction mixture was purged with nitrogen, filtered and concentrated in vacuo. The resulting oil was purified by reverse phase HPLC (water/acetonitrile gradient) to yield the title compound as a white powder. (9 mg, 75%) ¹ H NMR (CD₃ OD) δ1.41-1.58 (m, 2H,), 1.62-1.77 (m, 2H), 1.79-1.86 (m, 2H), 2.26 (s, 3H), 2.57-2.64 (m, 2H), 2.59 (s, 6H), 2.74-3.12 (m, 2H), 3.17-3.23 (m, 2H), 3.26-3.32 (m, 2H), 3.34-3.64 (m, 4H), 4.01-4.06 (m, 1H0, 4.70-4.80 (m, 1H), 6.95 (s, 2H), 8.24-8.26 (q, 1H), 8.81-8.89 (br s, 1H); Mass spectrum, ESI, (M+H)⁺ 536.5, base peak.

EXAMPLE 1001 3- 3- 3- (N-imidazolin-2-yl)amino!proxyloxy!isoxazol-5-yl!carbonylamino!propionic acid

A. Methyl 3- 3-(tert-butyloxycarbonylamino)propyloxy!-5-isoxazolecarboxylate:

Diethylazodicarboxylate (1.46 g, 8.39 mmol) was added dropwise to a mixture of methyl 3-hydroxy-5-isoxazolecarboxylate (1 g, 4.55 mmol), triphenylphosphine (1.46 g, 8.39 mmol), and 3-tert-butyloxycarbonylamino-1-propanol (1.50 g, 8.39 mmol) in anhydrous tetrahydrofuran (10 mL) at 0° C. under nitrogen. After 1 h remove the ice bath and warm to room temperature overnight. Dilute with ethyl acetate (75 mL) and wash with water (25 mL), saturated NaHCO₃ (25 mL), and brine (25 mL). Dry over MgSO₄ then evaporate the solvent in vacuo. The residue was chromatographed over silica gel (75 g, 25 to 60% ethyl acetate/hex) to give the title compound (1.95 g, 95%) as a waxy solid: ¹ H NMR (300 MHz, CDCl₃) δ6.53 (s, 1H), 4.74 (bs, 1H), 4.36 (t, 2H), 3.95 (s, 3H), 3.28 (q, 2H), 2.00 (m, 2H), 1.44 (s, 9H); MS (CI-NH₃) m/e 318 (M+NH₄)⁺ ; HRMS calc'd for C₁₃ H₂₀ N₂ O₆ +H: 301.1400, found 301.1403.

B. 3- 3-(tert-butyloxycarbonylamino)propyloxy!-5-isoxazole carboxylic acid:

Sodium Hydroxide (0.52 g, 13.0 mmol) in water (10 mL) was added in one portion to the product of Ex. 1001, Part A (1.95 g, 6.49 mmol) in methanol (20 mL) at room temperature. After 2 h the methanol was removed in vacuo and the residue was taken up in water (60 mL). The aqueous solution was washed with ether (30 mL, discard), then acidified to pH<2 with 10% HCl. Extraction with ethyl acetate (3×40 mL) was followed by washing the combined organic extracts with brine (40 mL) and drying over MgSO₄. The solvent was evaporated in vacuo to provide the desired acid (1.60 g, 86%) as a white solid: ¹ H NMR (300 MHz, CDCl₃) δ6.93 (s, 1H), 4.23 (t, 2H), 3.05 (q, 2H), 1.82 (m, 2H), 1.37 (s, 9H); MS (CI-NH₃) m/e 304 (M+NH₄)⁺ ; HRMS calc'd for C₁₂ H₁₈ N₂ O₆ +H: 287.1243, found 287.1259.

C. Ethyl 3- 3- 3-(tert-butyloxycarbonyl amino)propyloxy!isoxazol-5-ylcarbonylamino!propionate:

Diisopropyethylamine (0.68 g, 5.24 mmol) was added dropwise to the compound of Ex. 1001, Part B (0.5 g, 1.75 mmol), O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate (0.70 g, 1,83 mmol), and ethyl β-alanine hydrochloride (0.28 g, 1.83 mmol) in anhydrous dichloromethane (30 mL) at 0° C. under nitrogen. After the addition was completed the mixture was allowed to warm to room temperature and stirred for 7 h. The reaction was diluted with dichloromethane (75 mL) then washed with water (25 mL), 5% HCl (25 mL), saturated NaHCO₃ (25 mL), and brine (25 mL). After drying over MgSO₄ the solvent was evaporated in vacuo and the residue chromatographed on silica gel (30 g, 40 to 75% ethyl acetate/hexanes) to provide the title compound (0.23 g, 34%) as a viscous oil: ¹ H NMR (300 MHz, CDCl₃) δ 7.05 (bt, 1H), 6.49 (s, 1H), 4.68 (bs, 1H), 4.32 (t, 2H), 4.18 (q, 2H), 3.70 (q, 2H), 3.27 (q, 2H), 2.62 (t, 2H), 1.99 (m, 2H), 1.44 (s, 9H), 1.28 (t, 3H); MS (CI-NH₃) m/e 403 (M+NH₄)⁺ ; HRMS calc'd for C₁₇ H₂₇ N₃ O₇ +H: 386.1927, found 386.1909.

D. Ethyl 3- 3-(3-aminopropyloxy)isoxazol-5-ylcarbonylamino!propionate:

Trifluoroacetic acid (10 ml) was added in a slow stream to the compound of Ex. 1001, Part C (0.18 g 0.47 mmol) in dichloromethane (10 mL) at room temperature. After 45 min the trifluoroacetic acid was removed in vacuo and the residue was azotopically dried by evaporation in vacuo with toluene (20 mL), then place on a vacuum pump at 0.2 torr overnight. Upon dilution with chloroform the product crystallized out and was isolated as a white solid (0.14 g 75%): ¹ H NMR (300 MHz, CDCl₃) δ8.18 (bs, 3H), 7.80 (bt, 1H), 6.51 (s, 1H), 4.32 (m, 2H), 4.11 (q, 2H), 3.65 (q, 2H), 3.17 (m, 2H), 2.6 (t, 2H), 2.18 (m, 2H), 1.23 (t, 3H); MS (CI-NH₃) m/e 303 (M+NH₄)⁺ ; HRMS calc'd for C₁₂ H₂₉ N₃ O₅ +H: 286.1403, found 286.1404.

E. Ethyl 3- 3- 3-(imidazolin-2-yl amino)propyloxy!isoxazol-5-ylcarbonylamino!propionate:

The compound of Ex. 1001, part D (0.22 g, 0.77 mmol) and 2-methylmercapto-4,5-dihydroimidazole hydroiodide (0.38 g, 1.54 mmol) were combined in ethanol (20 mL) and heated to reflux for 2 hours. The solvent was removed in vacuo and the residue was chromatographed over silica gel (20 g, 9:3:1:0.6, chloroform, methanol, water, acetic acid, lower layer) to provide the desired product (0.13 g, %) as a clear viscous oil: ¹ H NMR (300 MHz, D₄ -MeOH) δ6.61 (s, 1H), 4.34 (t, 2H), 4.12 (q, 2H), 3.70 (s, 4H), 3.60 (t, 2H), 3.39 (t, 3H), 2.63 (t, 2H), 2.08 (m, 2H), 1,23 (t, 3H); MS (CI-NH₃) m/e 354 (M+H)⁺.

F. 3- 3- 3-(imidazolin-2-ylamino)propyloxy!isoxazol-5-ylcarbonylamino!propionic acid:

Lithium hydroxide (0.5M, 1 mL) was added to the compound of Ex. 1001, part E (0.13 g, 0.25 mmol) in dioxane (2 mL) at room temperature. After 1 h the solution was acidified with HCl in dioxane (4M, 2 mL) and the solvent was removed in vacuo. The residue was chromatographed on silica gel (10 g, 9:3:1:0.6, chloroform, methanol, water, acetic acid, lower layer) and the product fractions were evaporated in vacuo. The product was taken up in methanol (1 mL) and tetrahydrofuran was added slowly. The mixture was stirred overnight and the title product precipitated out as a white solid (32 mg): m.p. 144°-7° C.; ¹ H NMR (300 MHz, d₆ -DMSO) δ8.81 (bs, 2H), 6.77 (s, 1H), 6.76 (bs, 1H), 4.24 (m, 2H), 3.60 (q, 2H), 3.32 (m, 4H), 3.28 (m, 2H), 2.12 (m, 2H), 1.81 (m, 2H); MS (CI-NH₃) m/e 326 (M+H)⁺ ; HRMS calc'd for C₁₃ H₁₉ N₅ O₅ +H: 326.1464, found 326.1462.

EXAMPLE 1003 2(S)-benzyloxycarbonylamino-3- 3- 2- (N-imidazolin-2-yl)amino!ethoxy!isoxazol-5-yl!carbonylamino!propionic acid

A. 2-(tert-butyloxycarbonylamino)ethyl!methanesulfonate:

Methanesulfonyl chloride (8.2 g 71.6 mmol) in dichloromethane (45 mL) was added dropwise, over 8 min at ambient temperature to a stirring solution of 2-(t-butyloxycarbonylamino)ehtan-1-ol and TEA (9.83 g, 97.3 mmol) in dichloromethane (150 mL). After 2.5 hr the reaction mixture was washed with 1N HCl (2×50 mL), water (2×50 mL), and brine (50 mL) then dried over MgSO₄. The solution was filtered, and the solvent evaporated in vacuo to give the title compound (10.37 g, 67%). The resulting waxy solid could be used without further purification: ¹ H NMR (300 MHZ CDCl₃) δ 4.9(bs,1H), 4.3(t,2H), 3.3(q,2H) 3.04(s,1H).

B. 3- 3-(tert-butyloxycarbonylamino)ethyloxy!-5-isoxazole carboxylic acid:

The compound of Ex. 1003. Part A (10.37 g, 43.3 mmol) in dimethylformamide (25 mL) was added dropwise over 10 min to a stirring solution of methyl 3-hydroxy-5-isoxazolecarboxylate and sodium carbonate (5.83 g, 55 mmol). The reaction was heated to 80° C. for 3 h, then stirred at ambient temperture for 18 h. 10% Potassium carbonate (≈200 ml) was added to the reaction mixture and was stirred until the resulting precipitate dissolved. After cooling to 3° C. the solution was acidified to pH≅2 with concentrated HCl. The solid was collected by vacuum filtration, washed with water, then air dried to give the title compound (5.6 g, 47.5%) as a white solid: mp 246° C. vigorous bubbling ˜160°-170° C.; ¹ H NMR (300 MHz, CDCl₃) δ 6.51(s, 1H), 5.02(m, 1H), 4.35(t, 2H), 3.55(m, 2H), 1.43(s, 1H).

C. Methyl 2-benzyloxycarbonylamino-3- 3- 3-(tert-butyloxycarbonylamino)propyloxy!isoxazol-5-ylcarbonylamino!propionate:

Triethylamine (1.7 g, 16.7 mmol) was added in one portion to a mixture of the compound of Ex. 1003, Part B (1.68 g, 6.2 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.8 g, 9.3 mmol), the compound of Ex. 1004, part A (2.14 g, 7.4 mmol) and hydroxybenztriazole (260 mg 1.9 mmol) in anhydrous dimethylformamide (10 mL) at ambient temperature. After 14 h the reaction was diluted with 1N HCl to six time the volume. The acidic solution was then extracted with ethyl acetate (5×30 mL) and the combined organic extracts were washed with 10% K₂ CO₃ (3×50 ml), water (2×25 mL), and brine (25 mL). After drying over MgSO₄ the solvent was evaporated in vacuo. The crude product was triturated in 10% K₂ CO₃, filtered, washed with water then air dried. The product thus obtained (1.85 g 59%) was isolated as a white crystaline solid and could be used with out further purification: ¹ H NMR (300 MHz, DMSO) δ 8.95 (m, 1H), 7.78 (d, 1H), 7.36-7.31 (m, 5H) 7.05 (m, 1H), 6.79 (s, 1H) 5.09-4.99 (dd, 2H), 4.35-4.28 (q, 1H), 4,23-4.19 (t, 2H), 3.62 (s, 3H), 3.58-3.56 (m, 2H), 3.32-3.28 (m, 2H), 1.37 (s,9H); MS (DCI-NH₃) m/e 524 (M+NH₄)⁺.

D. 2-benzyloxycarbonylamino-3- 3-(2-tert-butyloxycarbonylamino)ethyloxy!isoxazol-5-yl carbonyl amino!propionic acid:

The compound of Ex. 1003, Part C (1.8 g, 3.6 mmol) was saponified using the procedure outlined for Ex. 1, Part C. The acid (0.81 g, 92%) was isolated as a brittle foam: ¹ H NMR (300 MHz, DMSO) δ8.92 (m, 1H) 7.62 (d, 1H) 7.35-7.30 (m,5H) 7.05 (m, 1H), 6.78 (s, 1H) 5.08-4.97 (dd, 2H) 4.27-4.19 (m, 3H) 3.60-3.55 (m 2H) 3.31-3.28 (m, 2H) 1.37 (s, 9H); MS (DCI-NH₃) m/e 510 (M+NH₄)⁺.

E. 3- 3-(2-aminoethyloxy!)isoxazol-5-ylcarbonylamino!-2-benzyloxycarbonylaminopropionic acid hydrochloride:

A solution of HCl in dioxane (4M, 10 mL) was added to the compound of Ex. 1003, Part C (1.6 g, 3.25 mmol) in 10 ml of dioxane. The mixture was stirred for 3 h at room temperature at which time a white solid had precipatated out. The product was filtered and washed with ether then dried overnight under vacuum (1.25 g, 90%): ¹ H NMR (300 MHz, DMSO) δ12.83 (bs, 1H), 9.06 (t, 1H), 8.24 (bs, 3H), 7.64 (d, 1H), 7.32 (m, 5H), 6.87 (s, 1H), 5.00 (s, 2H), 4.42 (t, 2H), 4.9.2 (m, 1H), 3.56 (m, 2H), 3.21 (m, 2H); MS (CI-NH₃); HRMS calc'd for C₁₇ H₂₁ N₄ O₇ +H: 393.1410, found 391.1391.

F. 2(S)-benzyloxycarbonylamino-3- 3- 2-(imidazolin-2-yl amino)ethyloxy!isoxazol-5-yl carbonyl amino!propionic acid:

2-methylthioimidazolinium iodide (114 mg, 0.5 mmol), the compound of Ex. 1003, Part E (0.10 g, 0.23 mmol), and dimethylamino pyridine (60 mg) were taken up in 1 ml of pyridine then heated to reflux for 2-3 min. The reaction was cooled to between 70°-80° C. and stirred for 24 hr. The solvent was removed in vacuo and the residue chromatographed on silica gel (20 g, 9:3:1:0.6, chloroform, methanol, water, and acetic acid, bottom layer). The product fractions were evaporated in vacuo and the resulting solid recrystallized from methanol/acetone to yield the title compound (33 mg, 31.2%) as a tan solid: mp 226.8° C. dec; ¹ H NMR (300 MHz, DMSO) δ8.82(m, 1H), 7.33 (m, 5H) 6.75 (d, 1H) 4.99 (s, 2H) 4.30-4.27(m, 2H), 3.58-3.52(m,7H), 3.33(m,1H); Mass Spec (ESI) m/e 461 (M+H)⁺ ; HRMS calc'd for C₂₀ H₂₅ N₆ O₇ +H: 461.1784, found 461.1789.

EXAMPLE 1004 2(S)-benzyloxycarbonylamino-3- 3- 3- (N-imidazolin-2-yl)amino!propyloxy!isoxazol-5-yl!carbonylamino!propionic acid

A. Methyl 3-amino-2(S)-(benzyloxycarbonyl)aminopropionate hydrochloride:

A solution of 4N HCl in dioxane (20 mL) was added to 3-amino-2-(benzyloxycarbonyl)aminopropanoic acid (2.39 g, 10 mmol) in methanol (20 mL) and the solution was stirred for 2 hours. The solvents was removed in vacuo to give the methyl ester (2.74 g, 95%) as a white solid product. NMR (DMSO-d₆): δ 8.38 (b, 3H); 7.96 (d, 1H); 7.38 (m, 5H); 5.05 (s, 2H); 4.44 (m, 1H); 3.66 (s, 3H); 3.14 (m, 2H)

B. Methyl 2-benzyloxycarbonylamino-3- 3- 3-(tert-butyloxycarbonylamino)propyloxy!isoxazol-5-ylcarbonylamino!propionate:

Diisopropylethylamine (0.54 g, 4.17 mmol) was added dropwise to a mixture of the compound of Ex. 1001, Part B (1.0 g, 3.48 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.70 g, 3.65 mmol), and the compound of Example 1004, Part A (1.0 g, 3.48 mmol) in anhydrous dimethylformamide (10 mL) at 0° C. under nitrogen. After 48 h the reaction was diluted with water (75 mL) then extraced with ethyl acetate (3×30 mL). The combined organic extracts were washed with water (2×25 mL) and brine (25 mL). After drying over MgSO₄ the sovent was evaporated in vacuo and the residue chromatographed on silica gel (30 g, 30 to 75% ethyl acetate/hexanes) to provide the title compound (0.90 g, 50%) as a viscous oil: ¹ H NMR (300 MHz, CDCl₃) δ 7.35 (m, 5H), 7.03 (bt, 1H), 6.49 (s, 1H), 5.78 (d, 1H), 5.13 (s, 1H), 4.73 (bt, 1H), 4.54 (q, 1H), 4.35 (t, 2H), 3.86 (t, 2H), 3.79 (s, 3H), 3.28 (q, 2H), 1.99 (m, 2H), 1.44 (s, 9H); MS (CI-NH₃) m/e 538 (M+NH₄)⁺ ; HRMS calc'd for C₂₄ H₃₂ N₄ O₉ +H: 521.2248, found 521.2266.

C. 3- 3- 3-(tert-butyloxycarbonylamino)propyloxy!isoxazol-5-yl carbonyl amino!-2-benzyloxycarbonylaminopropionic acid:

The compound of Ex. 1004, Part B (0.9 g, 1.73 mmol) was saponified using the procedure outlined for Example 1001, Part C. The acid (0.81 g, 92%) was isolated as a brittle foam: ¹ H NMR (300 MHz, DMSO) δ 8.91 (bt, 1H), 7.62 (d, 1H), 7.34 (m, 5H), 6.91 (bt, 1H), 6.78 (s, 1H), 5.03 (dd, 2H), 4.22 (m, 3H), 3.59 (m, 2H), 3.05 (q, 2H), 1.84 (m, 2H), 1.37 (s, 9H); MS (CI-NH₃) m/e 524 (M+NH₄)⁺ ; HRMS calc'd for C₂₃ H₃₀ N₄ O₉ +H: 507.2091, found 507.2105.

D. 3- 3-(3-aminopropyloxy!)isoxazol-5-ylcarbonylamino!-2(S)-benzyloxycarbonylaminopropionic acid hydrochloride:

A solution of HCl in dioxane (4M, 10 mL) was added to the compound of Example 1004 Part C (0.81 g, 1.60 mmol) dropwise. The mixture was stirred for 3 h at room temperature, at which time a white solid had precipatated out. The product was filtered then washed with ether and dried overnight under vacuum (0.58 g, 82%): ¹ H NMR (300 MHz, DMSO) δ12.83 (s, 1H), 8.98 (t, 1H), 7.88(bs, 3H), 7.64 (d, 1H), 7.34 (m, 5H), 6.83 (s, 1H), 5.03 (s, 2H), 4.31 (t, 2H), 4.27 (m, 1H), 3.40 (m, 2H), 2.92 (m, 2H), 2.04 (m, 2H); MS (CI-NH₃) m/e 407 (M+H)⁺ ; HRMS calc'd for C₁₈ H₂₂ N₄ O₇ +H: 407.1567, found 407.1553.

E. 3- 3- 3-(imidazolin-2-yl amino)propyloxy!isoxazol-5-yl carbonyl amino!-2-benzyloxycarbonylaminopropionic acid hydroiodide:

The compound of Ex. 1004, Part D (0.42 g, 0.95 mmol) and 2-methylmercapto-4,5-dihydroimidazole hydroiodide (0.35 g, 1.42 mmol) were combined in pyridine (2 mL) and heated to reflux for 4 h. Additional 2-methylmercapto-4,5-dihydroimidazole hydroiodide (0.35 g, 1.42 mmol) was added and the heating was continued for 2 h. The pyridine was removed in vacuo and the residue was chromatographed over silica gel (25 g, 9:3:1:0.6, chloroform, methanol, water, acetic acid, lower layer). The product fractions were combined and the solvent removed in vacuo. The residue was taken up in DMSO (1.5 ml) followed by addition of methanol (3 mL) then the slow addition of tetrahydrofuran (40 mL). The mixture was stirred for 30 min then filtered to provide the title compound (0.19 g, 34%) as a tan solid: m.p. 201°-2° C. (dec); ¹ H NMR 10.14 (bs, 1H), 9.64 (bs, 1H), 8.87 (bt, 1H), 7.34 (m, 5H), 6.78 (d, 1H), 6.75 (s, 1H), 5.00 (s, 2H), 4.22 (t, 2H), 3.85 (q, 1H), 3.56 (s, 4H), 3.55 (m, 1H), 3.23 (m, 3H), 1.92 (m, 2H); MS (esi) m/e 475 (M+H)⁺ ; HRMS calc'd for C₂₁ H₂₆ N₆ O₇ +H: 475.1941, found 475.1942.

Using the above procedures and modifications known to one skilled in the art of organic synthesis the following additional examples of Tables 1-5 may be prepared.

                                      TABLE 1                                      __________________________________________________________________________      ##STR34##                                                                     Ex. No.                                                                            R.sup.1 -U m n R.sup.8   R.sup.9   MS                                      __________________________________________________________________________      1  tetrahydropyrimidin-                                                                      3 1 H         H                                                     2-ylamino                                                                   2  tetrahydropyrimidin-                                                                      3 1 H         NHCbz     489.2                                       2-ylamino                                                                   3  tetrahydropyrimidin-                                                                      3 1 H         NHtBOC                                                2-ylamino                                                                   4  tetrahydropyrimidin-                                                                      3 1 H         NHCO.sub.2 -nBu                                       2-ylamino                                                                   5  tetrahydropyrimidin-                                                                      3 1 H         NHCO.sub.2 Et                                         2-ylamino                                                                   6  tetrahydropyrimidin-                                                                      3 1 H         NHCO.sub.2 Me                                         2-ylamino                                                                   7  tetrahydropyrimidin-                                                                      3 1 H         NHCO(CH.sub.2).sub.n Ph                               2-ylamino                                                                   8  tetrahydropyrimidin-                                                                      3 1 H         NHCOtBu                                               2-ylamino                                                                   9  tetrahydropyrimidin-                                                                      3 1 H         NHCO-n-C.sub.5 H.sub.11                               2-ylamino                                                                   10 tetrahydropyrimidin-                                                                      3 1 H         NHCO-n-C.sub.4 H.sub.9                                2-ylamino                                                                   11 tetrahydropyrimidin-                                                                      3 1 H         NHCOCH.sub.2 CH.sub.3                                 2-ylamino                                                                   12 tetrahydropyrimidin-                                                                      3 1 H         NHCOCH.sub.3                                          2-ylamino                                                                   13 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2 CH.sub.3                                   2-ylamino                                                                   14 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2 CH.sub.2 CH.sub.3                          2-ylamino                                                                   15 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2 n-Bu                                       2-ylamino                                                                   16 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2 Ph                                                                            495.2                                       2-ylamino                                                                   17 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-CH.sub.3)               2-ylamino                                                                   18 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2 Bn                                         2-ylamino                                                                   19 tetrahydropyrimidin-                                                                      3 1 H         NHCO(2-pyridyl)                                       2-ylamino                                                                   20 tetrahydropyrimidin-                                                                      3 1 H         NHCO(3-pyridyl)                                       2-ylamino                                                                   21 tetrahydropyrimidin-                                                                      3 1 H         NHCO(4-pyridyl)                                       2-ylamino                                                                   22 tetrahydropyrimidin-                                                                      3 1 H         NHCOCH.sub.2 (2-pyridyl)                              2-ylamino                                                                   23 tetrahydropyrimidin-                                                                      3 1 H         NHCOCH.sub.2 (3-pyridyl)                              2-ylamino                                                                   24 tetrahydropyrimidin-                                                                      3 1 H         NHCOCH.sub.2 (4-pyridyl)                              2-ylamino                                                                   25 tetrahydropyrimidin-                                                                      3 1 H         NHCO.sub.2 CH.sub.2 (2-pyridyl)                       2-ylamino                                                                   26 tetrahydropyrimidin-                                                                      3 1 H         NHCO.sub.2 CH.sub.2 (3-pyridyl)                       2-ylamino                                                                   27 tetrahydropyrimidin-                                                                      3 1 H         NHCO.sub.2 CH.sub.2 (4-pyridyl)                       2-ylamino                                                                   28 imidazolin-2-                                                                             3 1 H         H                                                     ylamino                                                                     29 imidazolin-2-                                                                             3 1 H         NHCbz                                                 ylamino                                                                     30 imidazolin-2-                                                                             3 1 H         NHtBOC                                                ylamino                                                                     31 imidazolin-2-                                                                             3 1 H         NHCO.sub.2 -nBu                                       ylamino                                                                     32 imidazolin-2-                                                                             3 1 H         NHCO.sub.2 Et                                         ylamino                                                                     33 imidazolin-2-                                                                             3 1 H         NHCO.sub.2 Me                                         ylamino                                                                     34 imidazolin-2-                                                                             3 1 H         NHCO(CH.sub.2).sub.n Ph                               ylamino                                                                     35 imidazolin-2-                                                                             3 1 H         NHCOtBu                                               ylamino                                                                     36 imidazolin-2-                                                                             3 1 H         NHCO-n-C.sub.5 H.sub.11                               ylamino                                                                     37 imidazolin-2-                                                                             3 1 H         NHCO-n-C.sub.4 H.sub.9                                ylamino                                                                     38 imidazolin-2-                                                                             3 1 H         NHCOCH.sub.2 CH.sub.3                                 ylamino                                                                     39 imidazolin-2-                                                                             3 1 H         NHCOCH.sub.3                                          ylamino                                                                     40 imidazolin-2-                                                                             3 1 H         NHSO.sub.2 CH.sub.3                                   ylamino                                                                     41 imidazolin-2-                                                                             3 1 H         NHSO.sub.2 CH.sub.2 CH.sub.3                          ylamino                                                                     42 imidazolin-2-                                                                             3 1 H         NHSO.sub.2 n-Bu                                       ylamino                                                                     43 imidazolin-2-                                                                             3 1 H         NHSO.sub.2 Ph                                         ylamino                                                                     44 imidazolin-2-                                                                             3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-CH.sub.3)               ylamino                                                                     45 imidazolin-2-                                                                             3 1 H         NHSO.sub.2 Bn                                         ylamino                                                                     46 imidazolin-2-                                                                             3 1 H         NHCO(2-pyridyl)                                       ylamino                                                                     47 imidazolin-2-                                                                             3 1 H         NHCO(3-pyridyl)                                       ylamino                                                                     48 imidazolin-2-                                                                             3 1 H         NHCO(4-pyridyl)                                       ylamino                                                                     49 imidazolin-2-                                                                             3 1 H         NHCOCH.sub.2 (2-pyridyl)                              ylamino                                                                     50 imidazolin-2-                                                                             3 1 H         NHCOCH.sub.2 (3-pyridyl)                              ylamino                                                                     51 imidazolin-2-                                                                             3 1 H         NHCOCH.sub.2 (4-pyridyl)                              ylamino                                                                     52 imidazolin-2-                                                                             3 1 H         NHCO.sub.2 CH.sub.2 (2-pyridyl)                       ylamino                                                                     53 imidazolin-2-                                                                             3 1 H         NHCO.sub.2 CH.sub.2 (3-pyridyl)                       ylamino                                                                     54 imidazolin-2-                                                                             3 1 H         NHCO.sub.2 CH.sub.2 (4-pyridyl)                       ylamino                                                                     55 tetrahydropyrimidin-                                                                      4 0 H         H                                                     2-ylamino                                                                   56 tetrahydropyrimidin-                                                                      4 0 H         NHCbz     489.3                                       2-ylamino                                                                   57 tetrahydropyrimidin-                                                                      4 0 H         NHtBOC                                                2-ylamino                                                                   58 tetrahydropyrimidin-                                                                      4 0 H         NHCO.sub.2 -nBu                                       2-ylamino                                                                   59 tetrahydropyrimidin-                                                                      4 0 H         NHCO.sub.2 Et                                         2-ylamino                                                                   60 tetrahydropyrimidin-                                                                      4 0 H         NHCO.sub.2 Me                                         2-ylamino                                                                   61 tetrahydropyrimidin-                                                                      4 0 H         NHCO(CH.sub.2).sub.n Ph                               2-ylamino                                                                   62 tetrahydropyrimidin-                                                                      4 0 H         NHCOtBu                                               2-ylamino                                                                   63 tetrahydropyrimidin-                                                                      4 0 H         NHCO-n-C.sub.5 H.sub.11                               2-ylamino                                                                   64 tetrahydropyrimidin-                                                                      4 0 H         NHCO-n-C.sub.4 H.sub.9                                2-ylamino                                                                   65 tetrahydropyrimidin-                                                                      4 0 H         NHCOCH.sub.2 CH.sub.3                                 2-ylamino                                                                   66 tetrahydropyrimidin-                                                                      4 0 H         NHCOCH.sub.3                                          2-ylamino                                                                   67 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2 CH.sub.3                                   2-ylamino                                                                   68 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2 CH.sub.2 CH.sub.3                          2-ylamino                                                                   69 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2 n-Bu                                       2-ylamino                                                                   70 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2 Ph                                         2-ylamino                                                                   71 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-CH.sub.3)               2-ylamino                                                                   72 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2 Bn                                         2-ylamino                                                                   73 tetrahydropyrimidin-                                                                      4 0 H         NHCO(2-pyridyl)                                       2-ylamino                                                                   74 tetrahydropyrimidin-                                                                      4 0 H         NHCO(3-pyridyl)                                       2-ylamino                                                                   75 tetrahydropyrimidin-                                                                      4 0 H         NHCO(4-pyridyl)                                       2-ylamino                                                                   76 tetrahydropyrimidin-                                                                      4 0 H         NHCOCH.sub.2 (2-pyridyl)                              2-ylamino                                                                   77 tetrahydropyrimidin-                                                                      4 0 H         NHCOCH.sub.2 (3-pyridyl)                              2-ylamino                                                                   78 tetrahydropyrimidin-                                                                      4 0 H         NHCOCH.sub.2 (4-pyridyl)                              2-ylamino                                                                   79 tetrahydropyrimidin-                                                                      4 0 H         NHCO.sub.2 CH.sub.2 (2-pyridyl)                       2-ylamino                                                                   80 tetrahydropyrimidin-                                                                      4 0 H         NHCO.sub.2 CH.sub.2 (3-pyridyl)                       2-ylamino                                                                   81 tetrahydropyrimidin-                                                                      4 0 H         NHCO.sub.2 CH.sub.2 (4-pyridyl)                       2-ylamino                                                                   82 imidazolin-2-                                                                             4 0 H         H                                                     ylamino                                                                     83 imidazolin-2-                                                                             4 0 H         NHCbz     475.3                                       ylamino                                                                     84 imidazolin-2-                                                                             4 0 H         NHtBOC                                                ylamino                                                                     85 imidazolin-2-                                                                             4 0 H         NHCO.sub.2 -nBu                                       ylamino                                                                     86 imidazolin-2-                                                                             4 0 H         NHCO.sub.2 Et                                         ylamino                                                                     87 imidazolin-2-                                                                             4 0 H         NHCO.sub.2 Me                                         ylamino                                                                     88 imidazolin-2-                                                                             4 0 H         NHCO(CH.sub.2).sub.n Ph                               ylamino                                                                     89 imidazolin-2-                                                                             4 0 H         NHCOtBu                                               ylamino                                                                     90 imidazolin-2-                                                                             4 0 H         NHCO-n-C.sub.5 H.sub.11                               ylamino                                                                     91 imidazolin-2-                                                                             4 0 H         NHCO-n-C.sub.4 H.sub.9                                ylamino                                                                     92 imidazolin-2-                                                                             4 0 H         NHCOCH.sub.2 CH.sub.3                                 ylamino                                                                     93 imidazolin-2-                                                                             4 0 H         NHCOCH.sub.3                                          ylamino                                                                     94 imidazolin-2-                                                                             4 0 H         NHSO.sub.2 CH.sub.3                                   ylamino                                                                     95 imidazolin-2-                                                                             4 0 H         NHSO.sub.2 CH.sub.2 CH.sub.3                          ylamino                                                                     96 imidazolin-2-                                                                             4 0 H         NHSO.sub.2 n-Bu                                       ylamino                                                                     97 imidazolin-2-                                                                             4 0 H         NHSO.sub.2 Ph                                         ylamino                                                                     98 imidazolin-2-                                                                             4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-CH.sub.3)               ylamino                                                                     99 imidazolin-2-                                                                             4 0 H         NHSO.sub.2 Bn                                         ylamino                                                                    100 imidazolin-2-                                                                             4 0 H         NHCO(2-pyridyl)                                       ylamino                                                                    101 imidazolin-2-                                                                             4 0 H         NHCO(3-pyridyl)                                       ylamino                                                                    102 imidazolin-2-                                                                             4 0 H         NHCO(4-pyridyl)                                       ylamino                                                                    103 imidazolin-2-                                                                             4 0 H         NHCOCH.sub.2 (2-pyridyl)                              ylamino                                                                    104 imidazolin-2-                                                                             4 0 H         NHCOCH.sub.2 (3-pyridyl)                              ylamino                                                                    105 imidazolin-2-                                                                             4 0 H         NHCOCH.sub.2 (4-pyridyl)                              ylamino                                                                    106 imidazolin-2-                                                                             4 0 H         NHCO.sub.2 CH.sub.2 (2-pyridyl)                       ylamino                                                                    107 imidazolin-2-                                                                             4 0 H         NHCO.sub.2 CH.sub.2 (3-pyridyl)                       ylamino                                                                    108 imidazolin-2-                                                                             4 0 H         NHCO.sub.2 CH.sub.2 (4-pyridyl)                       ylamino                                                                    109 tetrahydropyrimidin-                                                                      3 0 H         H                                                     2-ylamino                                                                  110 tetrahydropyrimidin-                                                                      3 0 H         NHCbz     475.3                                       2-ylamino                                                                  111 tetrahydropyrimidin-                                                                      3 0 H         NHtBOC                                                2-ylamino                                                                  112 tetrahydropyrimidin-                                                                      3 0 H         NHCO.sub.2 -nBu                                       2-ylamino                                                                  113 tetrahydropyrimidin-                                                                      3 0 H         NHCO.sub.2 Et                                         2-ylamino                                                                  114 tetrahydropyrimidin-                                                                      3 0 H         NHCO.sub.2 Me                                         2-ylamino                                                                  115 tetrahydropyrimidin-                                                                      3 0 H         NHCO(CH.sub.2).sub.n Ph                               2-ylamino                                                                  116 tetrahydropyrimidin-                                                                      3 0 H         NHCOtBu                                               2-ylamino                                                                  117 tetrahydropyrimidin-                                                                      3 0 H         NHCO-n-C.sub.5 H.sub.11                               2-ylamino                                                                  118 tetrahydropyrimidin-                                                                      3 0 H         NHCO-n-C.sub.4 H.sub.9                                2-ylamino                                                                  119 tetrahydropyrimidin-                                                                      3 0 H         NHCOCH.sub.2 CH.sub.3                                 2-ylamino                                                                  120 tetrahydropyrimidin-                                                                      3 0 H         NHCOCH.sub.3                                          2-ylamino                                                                  121 tetrahydropyrimidin-                                                                      3 0 H         NHSO.sub.2 CH.sub.3                                   2-ylamino                                                                  122 tetrahydropyrimidin-                                                                      3 0 H         NHSO.sub.2 CH.sub.2 CH.sub.3                          2-ylamino                                                                  123 tetrahydropyrimidin-                                                                      3 0 H         NHSO.sub.2 n-Bu                                       2-ylamino                                                                  124 tetrahydropyrimidin-                                                                      3 0 H         NHSO.sub.2 Ph                                                                            481.2                                       2-ylamino                                                                  125 tetrahydropyrimidin-                                                                      3 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-CH.sub.3)               2-ylamino                                                                  126 tetrahydropyrimidin-                                                                      3 0 H         NHSO.sub.2 Bn                                         2-ylamino                                                                  127 tetrahydropyrimidin-                                                                      3 0 H         NHCO(2-pyridyl)                                       2-ylamino                                                                  128 tetrahydropyrimidin-                                                                      3 0 H         NHCO(3-pyridyl)                                       2-ylamino                                                                  129 tetrahydropyrimidin-                                                                      3 0 H         NHCO(4-pyridyl)                                       2-ylamino                                                                  130 tetrahydropyrimidin-                                                                      3 0 H         NHCOCH.sub.2 (2-pyridyl)                              2-ylamino                                                                  131 tetrahydropyrimidin-                                                                      3 0 H         NHCOCH.sub.2 (3-pyridyl)                              2-ylamino                                                                  132 tetrahydropyrimidin-                                                                      3 0 H         NHCOCH.sub.2 (4-pyridyl)                              2-ylamino                                                                  133 tetrahydropyrimidin-                                                                      3 0 H         NHCO.sub.2 CH.sub.2 (2-pyridyl)                       2-ylamino                                                                  134 tetrahydropyrimidin-                                                                      3 0 H         NHCO.sub.2 CH.sub.2 (3-pyridyl)                       2-ylamino                                                                  135 tetrahydropyrimidin-                                                                      3 0 H         NHCO.sub.2 CH.sub.2 (4-pyridyl)                       2-ylamino                                                                  136 imidazolin-2-                                                                             3 0 H         H                                                     ylamino                                                                    137 imidazolin-2-                                                                             3 0 H         NHCbz     461.2                                       ylamino                                                                    138 imidazolin-2-                                                                             3 0 H         NHtBOC                                                ylamino                                                                    139 imidazolin-2-                                                                             3 0 H         NHCO.sub.2 -nBu                                       ylamino                                                                    140 imidazolin-2-                                                                             3 0 H         NHCO.sub.2 Et                                         ylamino                                                                    141 imidazolin-2-                                                                             3 0 H         NHCO.sub.2 Me                                         ylamino                                                                    142 imidazolin-2-                                                                             3 0 H         NHCO(CH.sub.2).sub.n Ph                               ylamino                                                                    143 imidazolin-2-                                                                             3 0 H         NHCOtBu                                               ylamino                                                                    144 imidazolin-2-                                                                             3 0 H         NHCO-n-C.sub.5 H.sub.11                               ylamino                                                                    145 imidazolin-2-                                                                             3 0 H         NHCO-n-C.sub.4 H.sub.9                                ylamino                                                                    146 imidazolin-2-                                                                             3 0 H         NHCOCH.sub.2 CH.sub.3                                 ylamino                                                                    147 imidazolin-2-                                                                             3 0 H         NHCOCH.sub.3                                          ylamino                                                                    148 imidazolin-2-                                                                             3 0 H         NHSO.sub.2 CH.sub.3                                   ylamino                                                                    149 imidazolin-2-                                                                             3 0 H         NHSO.sub.2 CH.sub.2 CH.sub.3                          ylamino                                                                    150 imidazolin-2-                                                                             3 0 H         NHSO.sub.2 n-Bu                                       ylamino                                                                    151 imidazolin-2-                                                                             3 0 H         NHSO.sub.2 Ph                                         ylamino                                                                    152 imidazolin-2-                                                                             3 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-CH.sub.3)               ylamino                                                                    153 imidazolin-2-                                                                             3 0 H         NHSO.sub.2 Bn                                         ylamino                                                                    154 imidazolin-2-                                                                             3 0 H         NHCO(2-pyridyl)                                       ylamino                                                                    155 imidazolin-2-                                                                             3 0 H         NHCO(3-pyridyl)                                       ylamino                                                                    156 imidazolin-2-                                                                             3 0 H         NHCO(4-pyridyl)                                       ylamino                                                                    157 imidazolin-2-                                                                             3 0 H         NHCOCH.sub.2 (2-pyridyl)                              ylamino                                                                    158 imidazolin-2-                                                                             3 0 H         NHCOCH.sub.2 (3-pyridyl)                              ylamino                                                                    159 imidazolin-2-                                                                             3 0 H         NHCOCH.sub.2 (4-pyridyl)                              ylamino                                                                    160 imidazolin-2-                                                                             3 0 H         NHCO.sub.2 CH.sub.2 (2-pyridyl)                       ylamino                                                                    161 imidazolin-2-                                                                             3 0 H         NHCO.sub.2 CH.sub.2 (3-pyridyl)                       ylamino                                                                    162 imidazolin-2-                                                                             3 0 H         NHCO.sub.2 CH.sub.2 (4-pyridyl)                       ylamino                                                                    172 pyridin-2-ylamino                                                                         3 1 H         NHCbz     484.2                                   173 pyridin-2-ylamino                                                                         3 1 H         NHCO.sub.2 -n-Bu                                  174 pyridin-2-ylamino                                                                         3 1 H         NHSO.sub.2 Ph                                     175 pyridin-2-ylamino                                                                         3 1 H         NHSO.sub.2 -Ph                                    176 pyridin-2-ylamino                                                                         4 0 H         NHCbz     484.4                                   177 pyridin-2-ylamino                                                                         4 0 H         NHCO.sub.2 -n-Bu                                  178 pyridin-2-ylamino                                                                         4 0 H         NHSO.sub.2 Ph                                     179 pyridin-2-ylamino                                                                         4 0 H         NHSO.sub.2 -nBu                                   180 pyridin-2-ylamino                                                                         3 0 H         NHCbz                                             181 pyridin-2-ylamino                                                                         3 0 H         NHCO.sub.2 -n-Bu                                  182 pyridin-2-ylamino                                                                         3 0 H         NHSO.sub.2 Ph                                     183 pyridin-2-ylamino                                                                         3 0 H         NHSO.sub.2 -nBu                                   184 imidazol-2-ylamino                                                                        3 1 H         NHCbz                                             185 imidazol-2-ylamino                                                                        3 1 H         NHCO.sub.2 -n-Bu                                  186 imidazol-2-ylamino                                                                        3 1 H         NHSO.sub.2 Ph                                     187 imidazol-2-ylamino                                                                        3 1 H         NHSO.sub.2 -nBu                                   188 imidazol-2-ylamino                                                                        4 0 H         NHCbz                                             189 imidazol-2-ylamino                                                                        4 0 H         NHCO.sub.2 -n-Bu                                  190 imidazol-2-ylamino                                                                        4 0 H         NHSO.sub.2 Ph                                     191 imidazol-2-ylamino                                                                        4 0 H         NHSO.sub.2 -nBu                                   192 imidazol-2-ylamino                                                                        3 0 H         NHCbz                                             193 imidazol-2-ylamino                                                                        3 0 H         NHCO.sub.2 -n-Bu                                  194 imidazol-2-ylamino                                                                        3 0 H         NHSO.sub.2 Ph                                     195 imidazol-2-ylamino                                                                        3 0 H         NHSO.sub.2 -nBu                                   196 thiazol-2-ylamino                                                                         3 1 H         NHCbz                                             197 2-aminopyridin-6-yl                                                                       3 1 H         NHCO.sub.2 -n-Bu                                  198 2-aminopyridin-6-yl                                                                       3 1 H         NHSO.sub.2 Ph                                     199 2-aminopyridin-6-yl                                                                       3 1 H         NHSO.sub.2 -nBu                                   200 2-aminopyridin-6-yl                                                                       4 0 H         NHCbz                                             201 2-aminopyridin-6-yl                                                                       4 0 H         NHCO.sub.2 -n-Bu                                  202 2-aminopyridin-6-yl                                                                       4 0 H         NHSO.sub.2 Ph                                     203 2-aminopyridin-6-yl                                                                       4 0 H         NHSO.sub.2 -nBu                                   204 2-aminopyridin-6-yl                                                                       3 0 H         NHCbz                                             205 2-aminopyridin-6-yl                                                                       3 0 H         NHCO.sub.2 -n-Bu                                  206 2-aminopyridin-6-yl                                                                       3 0 H         NHSO.sub.2 Ph                                     207 2-aminopyridin-6-yl                                                                       3 0 H         NHSO.sub.2 -nBu                                   208 2-aminopyridin-3-yl                                                                       2 0 H         NHCbz                                             209 2-aminopyridin-3-yl                                                                       2 0 H         NHCO.sub.2 -n-Bu                                  210 2-aminopyridin-3-yl                                                                       2 0 H         NHSO.sub.2 Ph                                     211 2-aminopyridin-3-yl                                                                       2 0 H         NHSO.sub.2 -nBu                                   212 2-aminothiazol-4-yl                                                                       3 1 H         NHCbz                                             213 2-aminothiazol-4-yl                                                                       3 1 H         NHCO.sub.2 -n-Bu                                  214 2-aminothiazol-4-yl                                                                       3 1 H         NHSO.sub.2 Ph                                     215 2-aminothiazol-4-yl                                                                       3 1 H         NHSO.sub.2 -nBu                                   216 2-aminothiazol-4-yl                                                                       4 0 H         NHCbz                                             217 2-aminothiazol-4-yl                                                                       4 0 H         NHCO.sub.2 -n-Bu                                  218 2-aminothiazol-4-yl                                                                       4 0 H         NHSO.sub.2 Ph                                     219 2-aminopyridin-6-yl                                                                       4 0 H         NHSO.sub.2 -nBu                                   220 2-aminothiazol-4-yl                                                                       3 0 H         NHCbz                                             221 2-aminothiazol-4-yl                                                                       3 0 H         NHCO.sub.2 -n-Bu                                  222 2-aminothiazol-4-yl                                                                       3 0 H         NHSO.sub.2 Ph                                     223 2-aminothiazol-4-yl                                                                       3 0 H         NHSO.sub.2 -nBu                                   224 2-aminothiazol-4-yl                                                                       3 1 H         NHCbz                                             225 2-aminothiazol-4-yl                                                                       3 1 H         NHCO.sub.2 -n-Bu                                  284 imidazolin-2-                                                                             2 2 H         NHCbz     475.3                                       ylamino                                                                    285 imidazolin-2-                                                                             2 2 H         NHCO.sub.2 -n-Bu                                      ylamino                                                                    286 imidazolin-2-                                                                             2 2 H         NHSO.sub.2 Ph                                         ylamino                                                                    287 imidazolin-2-                                                                             2 2 H         NHSO.sub.2 -nBu                                       ylamino                                                                    288 tetrahydropyrimidin-                                                                      2 2 H         NHCbz     489.4                                       2-ylamino                                                                  289 tetrahydropyrimidin-                                                                      2 2 H         NHCO.sub.2 -n-Bu                                      2-ylamino                                                                  290 tetrahydropyrimidin-                                                                      2 2 H         NHSO.sub.2 Ph                                         2-ylamino                                                                  291 tetrahydropyrimidin-                                                                      2 2 H         NHSO.sub.2 -nBu                                       2-ylamino                                                                  292 benzimidazol-2-                                                                           4 0 H         NHCbz                                                 ylamino                                                                    293 benzthiazol-2-                                                                            4 0 H         NHCbz                                                 ylamino                                                                    296 imidazol-4-ylamino                                                                        4 0 H         NHCbz                                             303 2-iminopyrrolidin-                                                                        3 1 H         NHCbz                                                 5-yl                                                                       304 2-iminopyrrolidin-                                                                        3 1 H         NHSO.sub.2 Ph                                         5-yl                                                                       305 2-iminopyrrolidin-                                                                        3 0 H         NHCbz                                                 5-yl                                                                       306 2-iminopyrrolidin-                                                                        3 0 H         NHSO.sub.2 Ph                                         5-yl                                                                       307 2-iminopyrrolidin-                                                                        2 1 H         NHCbz                                                 5-yl                                                                       308 2-iminopyrrolidin-                                                                        2 1 H         NHSO.sub.2 Ph                                         5-yl                                                                       309 2-iminopiperidin-6-                                                                       3 1 H         NHCbz                                                 yl                                                                         310 2-iminopiperidin-6-                                                                       3 1 H         NHSO.sub.2 Ph                                         yl                                                                         311 2-iminopiperidin-6-                                                                       3 0 H         NHCbz                                                 yl                                                                         312 2-iminopiperidin-6-                                                                       3 0 H         NHSO.sub.2 Ph                                         yl                                                                         313 2-iminopiperidin-6-                                                                       2 1 H         NHCbz                                                 yl                                                                         314 2-iminopiperidin-6-                                                                       2 1 H         NHSO.sub.2 Ph                                         yl                                                                         315 2-iminoazepin-7-yl                                                                        3 1 H         NHCbz                                             316 2-iminoazepin-7-yl                                                                        3 1 H         NHSO.sub.2 Ph                                     317 2-iminoazepin-7-yl                                                                        3 0 H         NHCbz                                             318 2-iminoazepin-7-yl                                                                        3 0 H         NHSO.sub.2 Ph                                     319 2-iminoazepin-7-yl                                                                        2 1 H         NHCbz                                             320 2-iminoazepin-7-yl                                                                        2 1 H         NHSO.sub.2 Ph                                     321 benzimidazol-2-                                                                           4 0 n-Bu      H                                                     ylamino                                                                    322 benzthiazol-2-                                                                            4 0 n-Bu      H                                                     ylamino                                                                    325 imidazol-4-ylamino                                                                        4 0 n-Bu      H                                                 335 thiazol-2-ylamino                                                                         4 0 H         NHCbz     490.4                                   340 imidazolin-2-                                                                             4 0 H         NHSO.sub.2 (2,4,6-                                    ylamino                  trimethylphenyl)                                  341 imidazolin-2-                                                                             4 0 H         NHSO.sub.2 (2,4,6-                                    ylamino                  trichlorophenyl)                                  342 imidazolin-2-                                                                             4 0 H         NHSO.sub.2 (2,6-                                      ylamino                  dichlorophenyl)                                   343 imidazolin-2-                                                                             4 0 H         NHSO.sub.2 (2-chloro-6-                               ylamino                  methylphenyl)                                     344 imidazolin-2-                                                                             4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)               ylamino                                                                    345 imidazolin-2-                                                                             4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                     ylamino                                                                    346 imidazolin-2-                                                                             4 0 H         NHSO2 4-(2,6-                                         ylamino                  dimethylphenyl)phenyl                             347 imidazolin-2-                                                                             4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                     ylamino                                                                    348 imidazolin-2-                                                                             4 0 H         NHSO.sub.2  4-(3,5-                                   ylamino                  dimethyl)isoxazolyl!                              349 imidazolin-2-                                                                             4 0 H         NHSO.sub.2 (1-napthyl)                                ylamino                                                                    350 imidazolin-2-                                                                             4 0 H         NHSO.sub.2 (2-napthyl)                                ylamino                                                                    351 imidazolin-2-                                                                             4 0 H         NHSO.sub.2 NHCH.sub.2 Ph                              ylamino                                                                    352 imidazolin-2-                                                                             4 0 H         NHSO.sub.2 NHPh                                       ylamino                                                                    353 imidazolin-2-                                                                             4 0 Ph        H                                                     ylamino                                                                    354 imidazolin-2-                                                                             4 0 phenylsulfonylamino                                                                      H                                                     ylamino        methyl                                                      355 imidazolin-2-                                                                             4 0 3-azabicyclo 3.2.2!                                                                      H                                                     ylamino        nonan-3-ylcarbonyl                                          356 imidazolin-2-                                                                             4 0 adamantan-1-yl                                                                           H                                                     ylamino        methylaminocarbonyl                                         357 imidazolin-2-                                                                             4 0 adamantan-1-yl                                                                           H                                                     ylamino        aminocarbonyl                                               358 imidazolin-2-                                                                             4 0 adamantan-2-yl                                                                           H                                                     ylamino        aminocarbonyl                                               359 imidazolin-2-                                                                             4 0 tetrahydroisoquinolin-                                                                   H                                                     ylamino        2-ylcarbonyl                                                360 imidazolin-2-                                                                             3 1 H         NHSO.sub.2 (2,4,6-                                    ylamino                  trimethylphenyl)                                  361 imidazolin-2-                                                                             3 1 H         NHSO.sub.2 (2,4,6-                                    ylamino                  trichlorophenyl)                                  362 imidazolin-2-                                                                             3 1 H         NHSO.sub.2 (2,6-                                      ylamino                  dichlorophenyl)                                   363 imidazolin-2-                                                                             3 1 H         NHSO.sub.2 (2-chloro-6-                               ylamino                  methylphenyl)                                     364 imidazolin-2-                                                                             3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)               ylamino                                                                    365 imidazolin-2-                                                                             3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                     ylamino                                                                    366 imidazolin-2-                                                                             3 1 H         NHSO2 4-(2,6-                                         ylamino                  dimethylphenyl)phenyl                             367 imidazolin-2-                                                                             3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                     ylamino                                                                    368 imidazolin-2-                                                                             3 1 H         NHSO.sub.2  4-(3,5-                                   ylamino                  dimethyl)isoxazolyl!                              369 imidazolin-2-                                                                             3 1 H         NHSO.sub.2 (1-napthyl)                                ylamino                                                                    370 imidazolin-2-                                                                             3 1 H         NHSO.sub.2 (2-napthyl)                                ylamino                                                                    371 imidazolin-2-                                                                             3 1 H         NHSO.sub.2 NHCH.sub.2 Ph                              ylamino                                                                    372 imidazolin-2-                                                                             3 1 H         NHSO.sub.2 NHPh                                       ylamino                                                                    373 imidazolin-2-                                                                             3 1 Ph        H                                                     ylamino                                                                    374 imidazolin-2-                                                                             3 1 phenylsulfonylamino                                                                      H                                                     ylamino        methyl                                                      375 imidazolin-2-                                                                             3 1 3-azabicyclo 3.2.2!                                                                      H                                                     ylamino        nonan-3-ylcarbonyl                                          376 imidazolin-2-                                                                             3 1 adamantan-1-yl                                                                           H                                                     ylamino        methylaminocarbonyl                                         377 imidazolin-2-                                                                             3 1 adamantan-1-yl                                                                           H                                                     ylamino        aminocarbonyl                                               378 imidazolin-2-                                                                             3 1 adamantan-2-yl                                                                           H                                                     ylamino        aminocarbonyl                                               379 imidazolin-2-                                                                             3 1 tetrahydroisoquinolin-                                                                   H                                                     ylamino        2-ylcarbonyl                                                380 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2 (2,4,6-                                    2-ylamino                trimethylphenyl)                                  381 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2 (2,4,6-                                    2-ylamino                trichlorophenyl)                                  382 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2 (2,6-                                      2-ylamino                dichlorophenyl)                                   383 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2 (2-chloro-6-                               2-ylamino                methylphenyl)                                     384 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)               2-ylamino                                                                  385 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                     2-ylamino                                                                  386 tetrahydropyrimidin-                                                                      4 0 H         NHSO2 4-(2,6-                                         2-ylamino                dimethylphenyl)phenyl                             387 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                     2-ylamino                                                                  388 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2  4-(3,5-                                   2-ylamino                dimethyl)isoxazolyl!                              389 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2 (1-napthyl)                                2-ylamino                                                                  390 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2 (2-napthyl)                                2-ylamino                                                                  391 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2 NHCH.sub.2 Ph                              2-ylamino                                                                  392 tetrahydropyrimidin-                                                                      4 0 H         NHSO.sub.2 NHPh                                       2-ylamino                                                                  393 tetrahydropyrimidin-                                                                      4 0 Ph        H                                                     2-ylamino                                                                  394 tetrahydropyrimidin-                                                                      4 0 phenylsulfonylamino                                                                      H                                                     2-ylamino      methyl                                                      395 tetrahydropyrimidin-                                                                      4 0 3-azabicyclo 3.2.2!                                                                      H                                                     2-ylamino      nonan-3-ylcarbonyl                                          396 tetrahydropyrimidin-                                                                      4 0 adamantan-1-yl                                                                           H                                                     2-ylamino      methylaminocarbonyl                                         397 tetrahydropyrimidin-                                                                      4 0 adamantan-1-yl                                                                           H                                                     2-ylamino      aminocarbonyl                                               398 tetrahydropyrimidin-                                                                      4 0 adamantan-2-yl                                                                           H                                                     2-ylamino      aminocarbonyl                                               399 tetrahydropyrimidin-                                                                      4 0 tetrahydroisoquinolin-                                                                   H                                                     2-ylamino      2-ylcarbonyl                                                400 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2 (2,4,6-                                    2-ylamino                trimethylphenyl)                                  401 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2 (2,4,6-                                    2-ylamino                trichlorophenyl)                                  402 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2 (2,6-                                      2-ylamino                dichlorophenyl)                                   403 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2 (2-chloro-6-                               2-ylamino                methylphenyl)                                     404 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)               2-ylamino                                                                  405 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                     2-ylamino                                                                  406 tetrahydropyrimidin-                                                                      3 1 H         NHSO2 4-(2,6-                                         2-ylamino                dimethylphenyl)phenyl                             407 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                     2-ylamino                                                                  408 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2  4-(3,5-                                   2-ylamino                dimethyl)isoxazolyl!                              409 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2 (1-napthyl)                                2-ylamino                                                                  410 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2 (2-napthyl)                                2-ylamino                                                                  411 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2 NHCH.sub.2 Ph                              2-ylamino                                                                  412 tetrahydropyrimidin-                                                                      3 1 H         NHSO.sub.2 NHPh                                       2-ylamino                                                                  413 tetrahydropyrimidin-                                                                      3 1 Ph        H                                                     2-ylamino                                                                  414 tetrahydropyrimidin-                                                                      3 1 phenylsulfonylamino                                                                      H                                                     2-ylamino      methyl                                                      415 tetrahydropyrimidin-                                                                      3 1 3-azabicyclo 3.2.2!                                                                      H                                                     2-ylamino      nonan-3-ylcarbonyl                                          416 tetrahydropyrimidin-                                                                      3 1 adamantan-1-yl                                                                           H                                                     2-ylamino      methylaminocarbonyl                                         417 tetrahydropyrimidin-                                                                      3 1 adamantan-1-yl                                                                           H                                                     2-ylamino      aminocarbonyl                                               418 tetrahydropyrimidin-                                                                      3 1 adamantan-2-yl                                                                           H                                                     2-ylamino      aminocarbonyl                                               419 tetrahydropyrimidin-                                                                      3 1 tetrahydroisoquinolin-                                                                   H                                                     2-ylamino      2-ylcarbonyl                                                420 imidazol-2-ylamino                                                                        4 0 H         NHSO.sub.2 (2,4,6-                                                             trimethylphenyl)                                  421 imidazol-2-ylamino                                                                        4 0 H         NHSO.sub.2 (2,4,6-                                                             trichlorophenyl)                                  422 imidazol-2-ylamino                                                                        4 0 H         NHSO.sub.2 (2,6-                                                               dichlorophenyl)                                   423 imidazol-2-ylamino                                                                        4 0 H         NHSO.sub.2 (2-chloro-6-                                                        methylphenyl)                                     424 imidazol-2-ylamino                                                                        4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)           425 imidazol-2-ylamino                                                                        4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                 426 imidazol-2-ylamino                                                                        4 0 H         NHSO2 4-(2,6-                                                                  dimethylphenyl)phenyl                             427 imidazol-2-ylamino                                                                        4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                 428 imidazol-2-ylamino                                                                        4 0 H         NHSO.sub.2  4-(3,5-                                                            dimethyl)isoxazolyl!                              429 imidazol-2-ylamino                                                                        4 0 H         NHSO.sub.2 (1-napthyl)                            430 imidazol-2-ylamino                                                                        4 0 H         NHSO.sub.2 (2-napthyl)                            431 imidazol-2-ylamino                                                                        4 0 H         NHSO.sub.2 NHCH.sub.2 Ph                          432 imidazol-2-ylamino                                                                        4 0 H         NHSO.sub.2 NHPh                                   433 imidazol-2-ylamino                                                                        4 0 Ph        H                                                 434 imidazol-2-ylamino                                                                        4 0 phenylsulfonylamino                                                                      H                                                                    methyl                                                      435 imidazol-2-ylamino                                                                        4 0 3-azabicyclo 3.2.2!                                                                      H                                                                    nonan-3-ylcarbonyl                                          436 imidazol-2-ylamino                                                                        4 0 adamantan-1-yl                                                                           H                                                                    methylaminocarbonyl                                         437 imidazol-2-ylamino                                                                        4 0 adamantan-1-yl                                                                           H                                                                    aminocarbonyl                                               438 imidazol-2-ylamino                                                                        4 0 adamantan-2-yl                                                                           H                                                                    aminocarbonyl                                               439 imidazol-2-ylamino                                                                        4 0 tetrahydroisoquinolin-                                                                   H                                                                    2-ylcarbonyl                                                440 imidazol-2-ylamino                                                                        3 1 H         NHSO.sub.2 (2,4,6-                                                             trimethylphenyl)                                  441 imidazol-2-ylamino                                                                        3 1 H         NHSO.sub.2 (2,4,6-                                                             trichlorophenyl)                                  442 imidazol-2-ylamino                                                                        3 1 H         NHSO.sub.2 (2,6-                                                               dichlorophenyl)                                   443 imidazol-2-ylamino                                                                        3 1 H         NHSO.sub.2 (2-chloro-6-                                                        methylphenyl)                                     444 imidazol-2-ylamino                                                                        3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)           445 imidazol-2-ylamino                                                                        3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                 446 imidazol-2-ylamino                                                                        3 1 H         NHSO2 4-(2,6-                                                                  dimethylphenyl)phenyl                             447 imidazol-2-ylamino                                                                        3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                 448 imidazol-2-ylamino                                                                        3 1 H         NHSO.sub.2  4-(3,5-                                                            dimethyl)isoxazolyl!                              449 imidazol-2-ylamino                                                                        3 1 H         NHSO.sub.2 (1-napthyl)                            450 imidazol-2-ylamino                                                                        3 1 H         NHSO.sub.2 (2-napthyl)                            451 imidazol-2-ylamino                                                                        3 1 H         NHSO.sub.2 NHCH.sub.2 Ph                          452 imidazol-2-ylamino                                                                        3 1 H         NHSO.sub.2 NHPh                                   453 imidazol-2-ylamino                                                                        3 1 Ph        H                                                 454 imidazol-2-ylamino                                                                        3 1 phenylsulfonylamino                                                                      H                                                                    methyl                                                      455 imidazol-2-ylamino                                                                        3 1 3-azabicyclo 3.2.2!                                                                      H                                                                    nonan-3-ylcarbonyl                                          456 imidazol-2-ylamino                                                                        3 1 adamantan-1-yl                                                                           H                                                                    methylaminocarbonyl                                         457 imidazol-2-ylamino                                                                        3 1 adamantan-1-yl                                                                           H                                                                    aminocarbonyl                                               458 imidazol-2-ylamino                                                                        3 1 adamantan-2-yl                                                                           H                                                                    aminocarbonyl                                               459 imidazol-2-ylamino                                                                        3 1 tetrahydroisoquinolin-                                                                   H                                                                    2-ylcarbonyl                                                460 2-aminoimidazol-4-                                                                        3 0 H         NHSO.sub.2 (2,4,6-                                    yl                       trimethylphenyl)                                  461 2-aminoimidazol-4-                                                                        3 0 H         NHSO.sub.2 (2,4,6-                                    yl                       trichlorophenyl)                                  462 2-aminoimidazol-4-                                                                        3 0 H         NHSO.sub.2 (2,6-                                      yl                       dichlorophenyl)                                   463 2-aminoimidazol-4-                                                                        3 0 H         NHSO.sub.2 (2-chloro-6-                               yl                       methylphenyl)                                     464 2-aminoimidazol-4-                                                                        3 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)               yl                                                                         465 2-aminoimidazol-4-                                                                        3 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                     yl                                                                         466 2-aminoimidazol-4-                                                                        3 0 H         NHSO.sub.2  4-(2,6-                                   yl                       dimethylphenyl)phenyl                             467 2-aminoimidazol-4-                                                                        3 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                     yl                                                                         468 2-aminoimidazol-4-                                                                        3 0 H         NHSO.sub.2  4-(3,5-                                   yl                       dimethyl)isoxazolyl!                              469 2-aminoimidazol-4-                                                                        3 0 H         NHSO.sub.2 (1-napthyl)                                yl                                                                         470 2-aminoimidazol-4-                                                                        3 0 H         NHSO.sub.2 (2-napthyl)                                yl                                                                         471 2-aminoimidazol-4-                                                                        3 0 H         NHSO.sub.2 NHCH.sub.2 Ph                              yl                                                                         472 2-aminoimidazol-4-                                                                        3 0 H         NHSO.sub.2 NHPh                                       yl                                                                         473 2-aminoimidazol-4-                                                                        3 0 Ph        H                                                     yl                                                                         474 2-aminoimidazol-4-                                                                        3 0 phenylsulfonylamino                                                                      H                                                     yl             methyl                                                      475 2-aminoimidazol-4-                                                                        3 0 3-azabicyclo 3.2.2!                                                                      H                                                     yl             nonan-3-ylcarbonyl                                          476 2-aminoimidazol-4-                                                                        3 0 adamantan-1-yl                                                                           H                                                     yl             methylaminocarbonyl                                         477 2-aminoimidazol-4-                                                                        3 0 adamantan-1-yl                                                                           H                                                     yl             aminocarbonyl                                               478 2-aminoimidazol-4-                                                                        3 0 adamantan-2-yl                                                                           H                                                     yl             aminocarbonyl                                               479 2-aminoimidazol-4-                                                                        3 0 tetrahydroisoquinolin-                                                                   H                                                     yl             2-ylcarbonyl                                                480 2-aminoimidazol-4-                                                                        2 1 H         NHSO.sub.2 (2,4,6-                                    yl                       trimethylphenyl)                                  481 2-aminoimidazol-4-                                                                        2 1 H         NHSO.sub.2 (2,4,6-                                    yl                       trichlorophenyl)                                  482 2-aminoimidazol-4-                                                                        2 1 H         NHSO.sub.2 (2,6-                                      yl                       dichlorophenyl)                                   483 2-aminoimidazol-4-                                                                        2 1 H         NHSO.sub.2 (2-chloro-6-                               yl                       methylphenyl)                                     484 2-aminoimidazol-4-                                                                        2 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)               yl                                                                         485 2-aminoimidazol-4-                                                                        2 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                     yl                                                                         486 2-aminoimidazol-4-                                                                        2 1 H         NHSO2 4-(2,6-                                         yl                       dimethylphenyl)phenyl                             487 2-aminoimidazol-4-                                                                        2 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                     yl                                                                         488 2-aminoimidazol-4-                                                                        2 1 H         NHSO.sub.2  4-(3,5-                                   yl                       dimethyl)isoxazolyl!                              489 2-aminoimidazol-4-                                                                        2 1 H         NHSO.sub.2 (1-napthyl)                                yl                                                                         490 2-aminoimidazol-4-                                                                        2 1 H         NHSO.sub.2 (2-napthyl)                                yl                                                                         491 2-aminoimidazol-4-                                                                        2 1 H         NHSO.sub.2 NHCH.sub.2 Ph                              yl                                                                         492 2-aminoimidazol-4-                                                                        2 1 H         NHSO.sub.2 NHPh                                       yl                                                                         493 2-aminoimidazol-4-                                                                        2 1 Ph        H                                                     yl                                                                         494 2-aminoimidazol-4-                                                                        2 1 phenylsulfonylamino                                                                      H                                                     yl             methyl                                                      495 2-aminoimidazol-4-                                                                        2 1 3-azabicyclo 3.2.2!                                                                      H                                                     yl             nonan-3-ylcarbonyl                                          496 2-aminoimidazol-4-                                                                        2 1 adamantan-1-yl                                                                           H                                                     yl             methylaminocarbonyl                                         497 2-aminoimidazol-4-                                                                        2 1 adamantan-1-yl                                                                           H                                                     yl             aminocarbonyl                                               498 2-aminoimidazol-4-                                                                        2 1 adamantan-2-yl                                                                           H                                                     yl             aminocarbonyl                                               499a                                                                               2-aminoimidazol-4-                                                                        2 1 tetrahydroisoquinolin-                                                                   H                                                     yl             2-ylcarbonyl                                                499b                                                                               benzimidazol-2-                                                                           4 0 H         NHSO.sub.2 (2,4,6-                                    ylamino                  trimethylphenyl)                                  499c                                                                               benzimidazol-2-                                                                           4 0 H         NHSO.sub.2 (2,4,6-                                    ylamino                  trichlorophenyl)                                  499d                                                                               benzimidazol-2-                                                                           4 0 H         NHSO.sub.2 (2,6-                                      ylamino                  dichlorophenyl)                                   499e                                                                               benzimidazol-2-                                                                           4 0 H         NHSO.sub.2 (2-chloro-6-                               ylamino                  methylphenyl)                                     499f                                                                               benzimidazol-2-                                                                           4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)               ylamino                                                                    499g                                                                               benzimidazol-2-                                                                           4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                     ylamino                                                                    499h                                                                               benzimidazol-2-                                                                           4 0 H         NHSO2 4-(2,6-                                         ylamino                  dimethylphenyl)phenyl                             499i                                                                               benzimidazol-2-                                                                           4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                     ylamino                                                                    499j                                                                               benzimidazol-2-                                                                           4 0 H         NHSO.sub.2  4-(3,5-                                   ylamino                  dimethyl)isoxazolyl!                              499k                                                                               benzimidazol-2-                                                                           4 0 H         NHSO.sub.2 (1-napthyl)                                ylamino                                                                    499l                                                                               benzimidazol-2-                                                                           4 0 H         NHSO.sub.2 (2-napthyl)                                ylamino                                                                    499m                                                                               benzimidazol-2-                                                                           4 0 H         NHSO.sub.2 NHCH.sub.2 Ph                              ylamino                                                                    499 benzimidazol-2-                                                                           4 0 H         NHSO.sub.2 NHPh                                       ylamino                                                                    499n                                                                               benzimidazol-2-                                                                           4 0 Ph        H                                                     ylamino                                                                    499o                                                                               benzimidazol-2-                                                                           4 0 phenylsulfonylamino                                                                      H                                                     ylamino        methyl                                                      499p                                                                               benzimidazol-2-                                                                           4 0 3-azabicyclo 3.2.2!                                                                      H                                                     ylamino        nonan-3-ylcarbonyl                                          499q                                                                               benzimidazol-2-                                                                           4 0 adamantan-1-yl                                                                           H                                                     ylamino        methylaminocarbonyl                                         499r                                                                               benzimidazol-2-                                                                           4 0 adamantan-1-yl                                                                           H                                                     ylamino        aminocarbonyl                                               499s                                                                               benzimidazol-2-                                                                           4 0 adamantan-2-yl                                                                           H                                                     ylamino        aminocarbonyl                                               499t                                                                               benzimidazol-2-                                                                           4 0 tetrahydroisoquinolin-                                                                   H                                                     ylamino        2-ylcarbonyl                                                499u                                                                               benzimidazol-2-                                                                           3 1 H         NHSO.sub.2 (2,4,6-                                    ylamino                  trimethylphenyl)                                  499v                                                                               benzimidazol-2-                                                                           3 1 H         NHSO.sub.2 (2,4,6-                                    ylamino                  trichlorophenyl)                                  499w                                                                               benzimidazol-2-                                                                           3 1 H         NHSO.sub.2 (2,6-                                      ylamino                  dichlorophenyl)                                   499x                                                                               benzimidazol-2-                                                                           3 1 H         NHSO.sub.2 (2-chloro-6-                               ylamino                  methylphenyl)                                     499y                                                                               benzimidazol-2-                                                                           3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)               ylamino                                                                    499z                                                                               benzimidazol-2-                                                                           3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                     ylamino                                                                    499aa                                                                              benzimidazol-2-                                                                           3 1 H         NHSO2 4-(2,6-                                         ylamino                  dimethylphenyl)phenyl                             499ab                                                                              benzimidazol-2-                                                                           3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                     ylamino                                                                    499ac                                                                              benzimidazol-2-                                                                           3 1 H         NHSO.sub.2  4-(3,5-                                   ylamino                  dimethyl)isoxazolyl!                              499ad                                                                              benzimidazol-2-                                                                           3 1 H         NHSO.sub.2 (1-napthyl)                                ylamino                                                                    499ae                                                                              benzimidazol-2-                                                                           3 1 H         NHSO.sub.2 (2-napthyl)                                ylamino                                                                    499af                                                                              benzimidazol-2-                                                                           3 1 H         NHSO.sub.2 NHCH.sub.2 Ph                              ylamino                                                                    499ag                                                                              benzimidazol-2-                                                                           3 1 H         NHSO.sub.2 NHPh                                       ylamino                                                                    499ah                                                                              benzimidazol-2-                                                                           3 1 Ph        H                                                     ylamino                                                                    499ai                                                                              benzimidazol-2-                                                                           3 1 phenylsulfonylamino                                                                      H                                                     ylamino        methyl                                                      499aj                                                                              benzimidazol-2-                                                                           3 1 3-azabicyclo 3.2.2!                                                                      H                                                     ylamino        nonan-3-ylcarbonyl                                          499ak                                                                              benzimidazol-2-                                                                           3 1 adamantan-1-yl                                                                           H                                                     ylamino        methylaminocarbonyl                                         499al                                                                              benzimidazol-2-                                                                           3 1 adamantan-1-yl                                                                           H                                                     ylamino        aminocarbonyl                                               499am                                                                              benzimidazol-2-                                                                           3 1 adamantan-2-yl                                                                           H                                                     ylamino        aminocarbonyl                                               499an                                                                              benzimidazol-2-                                                                           3 1 tetrahydroisoquinolin-                                                                   H                                                     ylamino        2-ylcarbonyl                                                499ao                                                                              4-methylimidazol-2-                                                                       4 0 H         NHSO.sub.2 (2,4,6-                                    ylamino                  trimethylphenyl)                                  499ap                                                                              4-methylimidazol-2-                                                                       4 0 H         NHSO.sub.2 (2,4,6-                                    ylamino                  trichlorophenyl)                                  499aq                                                                              4-methylimidazol-2-                                                                       4 0 H         NHSO.sub.2 (2,6-                                      ylamino                  dichlorophenyl)                                   499ar                                                                              4-methylimidazol-2-                                                                       4 0 H         NHSO.sub.2 (2-chloro-6-                               ylamino                  methylphenyl)                                     499as                                                                              4-methylimidazol-2-                                                                       4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)               ylamino                                                                    499at                                                                              4-methylimidazol-2-                                                                       4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                     ylamino                                                                    499au                                                                              4-methylimidazol-2-                                                                       4 0 H         NHSO2 4-(2,6-                                         ylamino                  dimethylphenyl)phenyl                             499av                                                                              4-methylimidazol-2-                                                                       4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                     ylamino                                                                    499aw                                                                              4-methylimidazol-2-                                                                       4 0 H         NHSO.sub.2  4-(3,5-                                   ylamino                  dimethyl)isoxazolyl)                              499ax                                                                              4-methylimidazol-2-                                                                       4 0 H         NHSO.sub.2 (1-napthyl)                                ylamino                                                                    499ay                                                                              4-methylimidazol-2-                                                                       4 0 H         NHSO.sub.2 (2-napthyl)                                ylamino                                                                    499az                                                                              4-methylimidazol-2-                                                                       4 0 H         NHSO.sub.2 NHCH.sub.2 Ph                              ylamino                                                                    499ba                                                                              4-methylimidazol-2-                                                                       4 0 H         NHSO.sub.2 NHPh                                       ylamino                                                                    499bb                                                                              4-methylimidazol-2-                                                                       4 0 Ph        H                                                     ylamino                                                                    499bc                                                                              4-methylimidazol-2-                                                                       4 0 phenylsulfonylamino                                                                      H                                                     ylamino        methyl                                                      499bd                                                                              4-methylimidazol-2-                                                                       4 0 3-azabicyclo 3.2.2!                                                                      H                                                     ylamino        nonan-3-ylcarbonyl                                          499be                                                                              4-methylimidazol-2-                                                                       4 0 adamantan-1-yl                                                                           H                                                     ylamino        methylaminocarbonyl                                         499bf                                                                              4-methylimidazol-2-                                                                       4 0 adamantan-1-yl                                                                           H                                                     ylamino        aminocarbonyl                                               499bg                                                                              4-methylimidazol-2                                                                        4 0 adamantan-2-yl                                                                           H                                                     ylamino        aminocarbonyl                                               499bh                                                                              4-methylimidazol-2-                                                                       4 0 tetrahydroisoquinolin-                                                                   H                                                     ylamino        2-ylcarbonyl                                                499bi                                                                              4-methylimidazol-2-                                                                       3 1 H         NHSO.sub.2 (2,4,6-                                    ylamino                  trimethylphenyl)                                  499bj                                                                              4-methylimidazol-2-                                                                       3 1 H         NHSO.sub.2 (2,4,6-                                    ylamino                  trichlorophenyl)                                  499bk                                                                              4-methylimidazol-2-                                                                       3 1 H         NHSO.sub.2 (2,6-                                      ylamino                  dichlorophenyl)                                   499bl                                                                              4-methylimidazol-2-                                                                       3 1 H         NHSO.sub.2 (2-chloro-6-                               ylamino                  methylphenyl)                                     499bm                                                                              4-methylimidazol-2-                                                                       3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)               ylamino                                                                    499bn                                                                              4-methylimidazol-2-                                                                       3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                     ylamino                                                                    499bo                                                                              4-methylimidazol-2-                                                                       3 1 H         NHSO2 4-(2,6-                                         ylamino                  dimethylphenyl)phenyl                             499bp                                                                              4-methylimidazol-2-                                                                       3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                     ylamino                                                                    499bq                                                                              4-methylimidazol-2-                                                                       3 1 H         NHSO.sub.2  4-(3,5-                                   ylamino                  dimethyl)isoxazolyl!                              499br                                                                              4-methylimidazol-2-                                                                       3 1 H         NHSO.sub.2 (1-napthyl)                                ylamino                                                                    499bs                                                                              4-methylimidazol-2-                                                                       3 1 H         NHSO.sub.2 (2-napthyl)                                ylamino                                                                    499bt                                                                              4-methylimidazol-2-                                                                       3 1 H         NHSO.sub.2 NHCH.sub.2 Ph                              ylamino                                                                    499bu                                                                              4-methylimidazol-2-                                                                       3 1 H         NHSO.sub.2 NHPh                                       ylamino                                                                    499bv                                                                              4-methylimidazol-2-                                                                       3 1 Ph        H                                                     ylamino                                                                    499bw                                                                              4-methylimidazol-2-                                                                       3 1 phenylsulfonylamino                                                                      H                                                     ylamino        methyl                                                      499bx                                                                              4-methylimidazol-2-                                                                       3 1 3-azabicyclo 3.2.2!                                                                      H                                                     ylamino        nonan-3-ylcarbonyl                                          499by                                                                              4-methylimidazol-2-                                                                       3 1 adamantan-1-yl                                                                           H                                                     ylamino        methylaminocarbonyl                                         499bz                                                                              4-methylimidazol-2-                                                                       3 1 adamantan-1-yl                                                                           H                                                     ylamino        aminocarbonyl                                               499ca                                                                              4-methylimidazol-2-                                                                       3 1 adamantan-2-yl                                                                           H                                                     ylamino        aminocarbonyl                                               499cb                                                                              4-methylimidazol-2-                                                                       3 1 tetrahydroisoquinolin-                                                                   H                                                     ylamino        2-ylcarbonyl                                                499cc                                                                              4,5-       4 0 H         NHSO.sub.2 (2,4,6-                                    dimethylimidazol-2-      trimethylphenyl)                                      ylamino                                                                    499cd                                                                              4,5-       4 0 H         NHSO.sub.2 (2,4,6-                                    dimethylimidazol-2-      trichlorophenyl)                                      ylamino                                                                    499ce                                                                              4,5-       4 0 H         NHSO.sub.2 (2,6-                                      dimethylimidazol-2-      dichlorophenyl)                                       ylamino                                                                    499cf                                                                              4,5-       4 0 H         NHSO.sub.2 (2-chloro-6-                               dimethylimidazol-2-      methylphenyl)                                         ylamino                                                                    499cg                                                                              4,5-       4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)               dimethylimidazol-2-                                                            ylamino                                                                    499ch                                                                              4,5-       4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                     dimethylimidazol-2-                                                            ylamino                                                                    499ci                                                                              4,5-       4 0 H         NHSO2 4-(2,6-                                         dimethylimidazol-2-      dimethylphenyl)phenyl                                 ylamino                                                                    499cj                                                                              4,5-       4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                     dimethylimidazol-2-                                                            ylamino                                                                    499ck                                                                              4,5-       4 0 H         NHSO.sub.2  4-(3,5-                                   dimethylimidazol-2-      dimethyl)isoxazolyl!                                  ylamino                                                                    499cl                                                                              4,5-       4 0 H         NHSO.sub.2 (1-napthyl)                                dimethylimidazol-2-                                                            ylamino                                                                    499cm                                                                              4,5-       4 0 H         NHSO.sub.2 (2-napthyl)                                dimethylimidazol-2-                                                            ylamino                                                                    499cn                                                                              4,5-       4 0 H         NHSO.sub.2 NHCH.sub.2 Ph                              dimethylimidazol-2-                                                            ylamino                                                                    499co                                                                              4,5-       4 0 H         NHSO.sub.2 NHPh                                       dimethylimidazol-2-                                                            ylamino                                                                    499cp                                                                              4,5-       4 0 Ph        H                                                     dimethylimidazol-2-                                                            ylamino                                                                    499cq                                                                              4,5-       4 0 phenylsulfonylamino                                                                      H                                                     dimethylimidazol-2-                                                                           methyl                                                          ylamino                                                                    499cr                                                                              4,5-       4 0 3-azabicyclo 3.2.2!                                                                      H                                                     dimethylimidazol-2-                                                                           nonan-3-ylcarbonyl                                              ylamino                                                                    499cs                                                                              4,5-       4 0 adamantan-1-yl                                                                           H                                                     dimethylimidazol-2-                                                                           methylaminocarbonyl                                             ylamino                                                                    499ct                                                                              4,5-       4 0 adamantan-1-yl                                                                           H                                                     dimethylimidazol-2-                                                                           aminocarbonyl                                                   ylamino                                                                    499cu                                                                              4,5-       4 0 adamantan-2-yl                                                                           H                                                     dimethylimidazol-2-                                                                           aminocarbonyl                                                   ylamino                                                                    499cv                                                                              4,5-       4 0 tetrahydroisoquinolin-                                                                   H                                                     dimethylimidazol-2-                                                                           2-ylcarbonyl                                                    ylamino                                                                    499cw                                                                              4,5-       3 1 H         NHSO.sub.2 (2,4,6-                                    dimethylimidazol-2-      trimethylphenyl)                                      ylamino                                                                    499cx                                                                              4,5-       3 1 H         NHSO.sub.2 (2,4,6-                                    dimethylimidazol-2-      trichlorophenyl)                                      ylamino                                                                    499cy                                                                              4,5-       3 1 H         NHSO.sub.2 (2,6-                                      dimethylimidazol-2-      dichlorophenyl)                                       ylamino                                                                    499cz                                                                              4,5-       3 1 H         NHSO.sub.2 (2-chloro-6-                               dimethylimidazol-2-      methylphenyl)                                         ylamino                                                                    499da                                                                              4,5-       3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)               dimethylimidazol-2-                                                            ylamino                                                                    499db                                                                              4,5-       3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                     dimethylimidazol-2-                                                            ylamino                                                                    499dc                                                                              4,5-       3 1 H         NHSO2 4-(2,6-                                         dimethylimidazol-2-      dimethylphenyl)phenyl                                 ylamino                                                                    499de                                                                              4,5-       3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                     dimethylimidazol-2-                                                            ylamino                                                                    499df                                                                              4,5-       3 1 H         NHSO.sub.2  4-(3,5-                                   dimethylimidazol-2-      dimethyl)isoxazolyl!                                  ylamino                                                                    499dg                                                                              4,5-       3 1 H         NHSO.sub.2 (1-napthyl)                                dimethylimidazol-2-                                                            ylamino                                                                    499dh                                                                              4,5-       3 1 H         NHSO.sub.2 (2-napthyl)                                dimethylimidazol-2-                                                            ylamino                                                                    499di                                                                              4,5-       3 1 H         NHSO.sub.2 NHCH.sub.2 Ph                              dimethylimidazol-2-                                                            ylamino                                                                    499dj                                                                              4,5-       3 1 H         NHSO.sub.2 NHPh                                       dimethylimidazol-2-                                                            ylamino                                                                    499dk                                                                              4,5-       3 1 Ph        H                                                     dimethylimidazol-2-                                                            ylamino                                                                    499dl                                                                              4,5-       3 1 phenylsulfonylamino                                                                      H                                                     dimethylimidazol-2-                                                                           methyl                                                          ylamino                                                                    499dm                                                                              4,5-       3 1 3-azabicyclo 3.2.2!                                                                      H                                                     dimethylimidazol-2-                                                                           nonan-3-ylcarbonyl                                              ylamino                                                                    499dn                                                                              4,5-       3 1 adamantan-1-yl                                                                           H                                                     dimethylimidazol-2-                                                                           methylaminocarbonyl                                             ylamino                                                                    499do                                                                              4,5-       3 1 adamantan-1-yl                                                                           H                                                     dimethylimidazol-2-                                                                           aminocarbonyl                                                   ylamino                                                                    499dp                                                                              4,5-       3 1 adamantan-2-yl                                                                           H                                                     dimethylimidazol-2-                                                                           aminocarbonyl                                                   ylamino                                                                    499dq                                                                              4,5-       3 1 tetrahydroisoquinolin-                                                                   H                                                     dimethylimidazol-2-                                                                           2-ylcarbonyl                                                    ylamino                                                                    499dr                                                                              4,5,6,7-   4 0 H         NHSO.sub.2 (2,4,6-                                    tetrahydrobenzimidazol-  trimethylphenyl)                                      2-ylamino                                                                  499ds                                                                              4,5,6,7-   4 0 H         NHSO.sub.2 (2,4,6-                                    tetrahydrobenzimidazol-  trichloropbenyl)                                      2-ylamino                                                                  499dt                                                                              4,5,6,7-   4 0 H         NHSO.sub.2 (2,6-                                      tetrahydrobenzimidazol-  dichlorophenyl)                                       2-ylamino                                                                  499du                                                                              4,S,6,7-   4 0 H         NHSO.sub.2 (2-chloro-6-                               tetrahydrobenzimidazol-  methylphenyl)                                         2-ylamino                                                                  499dv                                                                              4,5,6,7-   4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)               tetrahydrobenzimidazol-                                                        2-ylamino                                                                  499dw                                                                              4,5,6,7-   4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                     tetrahydrobenzimidazol-                                                        2-ylamino                                                                  499dx                                                                              4,5,6,7-   4 0 H         NHSO2 4-(2,6-                                         tetrahydrobenzimidazol-  dimethylphenyl)phenyl                                 2-ylamino                                                                  499dy                                                                              4,5,6,7-   4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                     tetrahydrobenzimidazol-                                                        2-ylamino                                                                  499dz                                                                              4,5,6,7-   4 0 H         NHSO.sub.2  4-(3,5-                                   tetrahydrobenzimidazol-  dimethyl)isoxazolyl!                                  2-ylamino                                                                  499ea                                                                              4,5,6,7-   4 0 H         NHSO.sub.2 (1-napthyl)                                tetrahydrobenzimidazol-                                                        2-ylamino                                                                  499eb                                                                              4,5,6,7-   4 0 H         NHSO.sub.2 (2-napthyl)                                tetrahydrobenzimidazol-                                                        2-ylamino                                                                  499ec                                                                              4,5,6,7-   4 0 H         NHSO.sub.2 NHCH.sub.2 Ph                              tetrahydrobenzimidazol-                                                        2-ylamino                                                                  499ed                                                                              4,5,6,7-   4 0 H         NHSO.sub.2 NHPh                                       tetrahydrobenzimidazol-                                                        2-ylamino                                                                  499ee                                                                              4,5,6,7-   4 0 Ph        H                                                     tetrahydrobenzimidazol-                                                        2-ylamino                                                                  499ef                                                                              4,5,6,7-   4 0 phenylsulfonylamino                                                                      H                                                     tetrahydrobenzimidazol-                                                                       methyl                                                          2-ylamino                                                                  499eg                                                                              4,5,6,7-   4 0 3-azabicyclo 3.2.2!                                                                      H                                                     tetrahydrobenzimidazol-                                                                       nonan-3-ylcarbonyl                                              2-ylamino                                                                  499eh                                                                              4,5,6,7-   4 0 adamantan-1-yl                                                                           H                                                     tetrahydrobenzimidazol-                                                                       methylaminocarbonyl                                             2-ylamino                                                                  499ei                                                                              4,5,6,7-   4 0 adamantan-1-yl                                                                           H                                                     tetrahydrobenzimidazol-                                                                       aminocarbonyl                                                   2-ylamino                                                                  499ej                                                                              4,5,6,7-   4 0 adamantan-2-yl                                                                           H                                                     tetrahydrobenzimidazol-                                                                       aminocarbonyl                                                   2-ylamino                                                                  499ek                                                                              4,5,6,7-   4 0 tetrahydroisoquinolin-                                                                   H                                                     tetrahydrobenzimidazol-                                                                       2-ylcarbonyl                                                    2-ylamino                                                                  499el                                                                              4,5,6,7-   3 1 H         NHSO.sub.2 (2,4,6-                                    tetrahydrobenzimidazol-  trimethylphenyl)                                      2-ylamino                                                                  499em                                                                              4,5,6,7-   3 1 H         NHSO.sub.2 (2,4,6-                                    tetrahydrobenzimidazol-  trichlorophenyl)                                      2-ylamino                                                                  499en                                                                              4,5,6,7-   3 1 H         NHSO.sub.2 (2,6-                                      tetrahydrobenzimidazol-  dichlorophenyl)                                       2-ylamino                                                                  499eo                                                                              4,5,6,7-   3 1 H         NHSO.sub.2 (2-chloro-6-                               tetrahydrobenzimidazol-  methylphenyl)                                         2-ylamino                                                                  499ep                                                                              4,5,6,7-   3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)               tetrahydrobenzimidazol-                                                        2-ylamino                                                                  499eq                                                                              4,5,6,7-   3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                     tetrahydrobenzimidazol-                                                        2-ylamino                                                                  499er                                                                              4,5,6,7-   3 1 H         NHSO2 4-(2,6-                                         tetrahydrobenzimidazol-  dimethylphenyl)phenyl                                 2-ylamino                                                                  499es                                                                              4,5,6,7-   3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                     tetrahydrobenzimidazol-                                                        2-ylamino                                                                  499et                                                                              4,5,6,7-   3 1 H         NHSO.sub.2  4-(3,5-                                   tetrahydrobenzimidazol-  dimethyl)isoxazolyl!                                  2-ylamino                                                                  499eu                                                                              4,5,6,7-   3 1 H         NHSO.sub.2 (1-napthyl)                                tetrahydrobenzimidazol-                                                        2-ylamino                                                                  499ev                                                                              4,5,6,7-   3 1 H         NHSO.sub.2 (2-napthyl)                                tetrahydrobenzimidazol-                                                        2-ylamino                                                                  499ew                                                                              4,5,6,7-   3 1 H         NHSO.sub.2 NHCH.sub.2 Ph                              tetrahydrobenzimidazol-                                                        2-ylamino                                                                  499ex                                                                              4,5,6,7-   3 1 H         NHSO.sub.2 NHPh                                       tetrahydrobenzimidazol-                                                        2-ylamino                                                                  499ey                                                                              4,5,6,7-   3 1 Ph        H                                                     tetrahydrobenzimidazol-                                                        2-ylamino                                                                  499ez                                                                              4,5,6,7-   3 1 phenylsulfonylamino                                                                      H                                                     tetrahydrobenzimidazol-                                                                       methyl                                                          2-ylamino                                                                  499fa                                                                              4,5,6,7-   3 1 3-azabicyclo 3.2.2!                                                                      H                                                     tetrahydrobenzimidazol-                                                                       nonan-3-ylcarbonyl                                              2-ylamino                                                                  499fb                                                                              4,5,6,7-   3 1 adamantan-1-yl                                                                           H                                                     tetrahydrobenzimidazol-                                                                       methylaminocarbonyl                                             2-ylamino                                                                  499fc                                                                              4,5,6,7-   3 1 adamantan-1-yl                                                                           H                                                     tetrahydrobenzimidazol-                                                                       aminocarbonyl                                                   2-ylamino                                                                  499fd                                                                              4,5,6,7-   3 1 adamantan-2-yl                                                                           H                                                     tetrahydrobenzimidazol-                                                                       aminocarbonyl                                                   2-ylamino                                                                  499fe                                                                              4,5,6,7-   3 1 tetrahydroisoquinolin-                                                                   H                                                     tetrahydrobenzimidazol-                                                                       2-ylcarbonyl                                                    2-ylamino                                                                  499ff                                                                              pyridin-2-ylamino                                                                         4 0 H         NHSO.sub.2 (2,4,6-                                                             trimethylphenyl)                                  499fg                                                                              pyridin-2-ylamino                                                                         4 0 H         NHSO.sub.2 (2,4,6-                                                             trichlorophenyl)                                  499fh                                                                              pyridin-2-ylamino                                                                         4 0 H         NHSO.sub.2 (2,6-                                                               dichlorophenyl)                                   499fi                                                                              pyridin-2-ylamino                                                                         4 0 H         NHSO.sub.2 (2-chloro-6-                                                        methylphenyl)                                     499fj                                                                              pyridin-2-ylamino                                                                         4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)           499fk                                                                              pyridin-2-ylamino                                                                         4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                 499fl                                                                              pyridin-2-ylamino                                                                         4 0 H         NHSO2 4-(2,6-                                                                  dimethylphenyl)phenyl                             499fm                                                                              pyridin-2-ylamino                                                                         4 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                 499fn                                                                              pyridin-2-ylamino                                                                         4 0 H         NHSO.sub.2  4-(3,5-                                                            dimethyl)isoxazolyl!                              499of                                                                              pyridin-2-ylamino                                                                         4 0 H         NHSO.sub.2 (1-napthyl)                            499fp                                                                              pyridin-2-ylamino                                                                         4 0 H         NHSO.sub.2 (2-napthyl)                            499fq                                                                              pyridin-2-ylamino                                                                         4 0 H         NHSO.sub.2 NHCH.sub.2 Ph                          499fr                                                                              pyridin-2-ylamino                                                                         4 0 H         NHSO.sub.2 NHPh                                   499fs                                                                              pyridin-2-ylamino                                                                         4 0 Ph        H                                                 499ft                                                                              pyridin-2-ylamino                                                                         4 0 phenylsulfonylamino                                                                      H                                                                    methyl                                                      499fu                                                                              pyridin-2-ylamino                                                                         4 0 3-azabicyclo 3.2.2!                                                                      H                                                                    nonan-3-ylcarbonyl                                          499fv                                                                              pyridin-2-ylamino                                                                         4 0 adamantan-1-yl                                                                           H                                                                    methylaminocarbonyl                                         499fw                                                                              pyridin-2-ylamino                                                                         4 0 adamantan-1-yl                                                                           H                                                                    aminocarbonyl                                               499fy                                                                              pyridin-2-ylamino                                                                         4 0 adamantan-2-yl                                                                           H                                                                    aminocarbonyl                                               499fz                                                                              pyridin-2-ylamino                                                                         4 0 tetrahydroisoquinolin-                                                                   H                                                                    2-ylcarbonyl                                                499ga                                                                              pyridin-2-ylamino                                                                         3 1 H         NHSO.sub.2 (2,4,6-                                                             trimethylphenyl)                                  499gb                                                                              pyridin-2-ylamino                                                                         3 1 H         NHSO.sub.2 (2,4,6-                                                             trichlorophenyl)                                  499gc                                                                              pyridin-2-ylamino                                                                         3 1 H         NHSO.sub.2 (2,6-                                                               dichlorophenyl)                                   499gd                                                                              pyridin-2-ylamino                                                                         3 1 H         NHSO.sub.2 (2-chloro-6-                                                        methylphenyl)                                     499ge                                                                              pyridin-2-ylamino                                                                         3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)           499gf                                                                              pyridin-2-ylamino                                                                         3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                 499gh                                                                              pyridin-2-ylamino                                                                         3 1 H         NHSO2 4-(2,6-                                                                  dimethylphenyl)phenyl                             499gi                                                                              pyridin-2-ylamino                                                                         3 1 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                 499gk                                                                              pyridin-2-ylamino                                                                         3 1 H         NHSO.sub.2  4-(3,5-                                                            dimethyl)isoxazolyl!                              499gl                                                                              pyridin-2-ylamino                                                                         3 1 H         NHSO.sub.2 (1-napthyl)                            499gm                                                                              pyridin-2-ylamino                                                                         3 1 H         NHSO.sub.2 (2-napthyl)                            499gn                                                                              pyridin-2-ylamino                                                                         3 1 H         NHSO.sub.2 NHCH.sub.2 Ph                          499go                                                                              pyridin-2-ylamino                                                                         3 1 H         NHSO.sub.2 NHPh                                   499gp                                                                              pyridin-2-ylamino                                                                         3 1 Ph        H                                                 499gq                                                                              pyridin-2-ylamino                                                                         3 1 phenylsulfonylamino                                                                      H                                                                    methyl                                                      499gr                                                                              pyridin-2-ylamino                                                                         3 1 3-azabicyclo 3.2.2!                                                                      H                                                                    nonan-3-ylcarbonyl                                          499gs                                                                              pyridin-2-ylamino                                                                         3 1 adamantan-1-yl                                                                           H                                                                    methylaminocarbonyl                                         499gt                                                                              pyridin-2-ylamino                                                                         3 1 adamantan-1-yl                                                                           H                                                                    aminocarbonyl                                               499gu                                                                              pyridin-2-ylamino                                                                         3 1 adamantan-2-yl                                                                           H                                                                    aminocarbonyl                                               499gv                                                                              pyridin-2-ylamino                                                                         3 1 tetrahydroisoquinolin-                                                                   H                                                                    2-ylcarbonyl                                                499gw                                                                              benzimidazol-2-                                                                           0 0 H         NHSO.sub.2 (2,4,6-                                    ylmethylaminocarbonyl    trimethylphenyl)                                  499gx                                                                              benzimidazol-2-                                                                           0 0 H         NHSO.sub.2 (2,4,6-                                    ylmethylaminocarbonyl    trichlorophenyl)                                  499gy                                                                              benzimidazol-2-                                                                           0 0 H         NHSO.sub.2 (2,6-                                      ylmethylaminocarbonyl    dichlorophenyl)                                   499gz                                                                              benzimidazol-2-                                                                           0 0 H         NHSO.sub.2 (2-chloro-6-                               ylmethylaminocarbonyl    methylphenyl)                                     499ha                                                                              benzimidazol-2-                                                                           0 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)               ylmethylaminocarbonyl                                                      499hb                                                                              benzimidazol-2-                                                                           0 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                     ylmethylaminocarbonyl                                                      499hc                                                                              benzimidazol-2-                                                                           0 0 H         NHSO2 4-(2,6-                                         ylmethylaminocarbonyl    dimethylphenyl)phenyl                             499hd                                                                              benzimidazol-2-                                                                           0 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                     ylmethylaminocarbonyl                                                      499he                                                                              benzimidazol-2-                                                                           0 0 H         NHSO.sub.2  4-(3,5-                                   ylmethylaminocarbonyl    dimethyl)isoxazolyl!                              499hf                                                                              benzimidazol-2-                                                                           0 0 H         NHSO.sub.2 (1-napthyl)                                ylmethylaminocarbonyl                                                      499hg                                                                              benzimidazol-2-                                                                           0 0 H         NHSO.sub.2 (2-napthyl)                                ylmethylaminocarbonyl                                                      499hi                                                                              benzimidazol-2-                                                                           0 0 H         NHSO.sub.2 NHCH.sub.2 Ph                              ylmethylaminocarbonyl                                                      499hj                                                                              benzimidazol-2-                                                                           0 0 H         NHSO.sub.2 NHPh                                       ylmethylaminocarbonyl                                                      499hk                                                                              benzimidazol-2-                                                                           0 0 Ph        H                                                     ylmethylaminocarbonyl                                                      499hl                                                                              benzimidazol-2-                                                                           0 0 phenylsulfonylamino                                                                      H                                                     ylmethylaminocarbonyl                                                                         methyl                                                      499hm                                                                              benzimidazol-2-                                                                           0 0 3-azabicyclo 3.2.2!                                                                      H                                                     ylmethylaminocarbonyl                                                                         nonan-3-ylcarbonyl                                          499hn                                                                              benzimidazol-2-                                                                           0 0 adamantan-1-yl                                                                           H                                                     ylmethylaminocarbonyl                                                                         methylaminocarbonyl                                         499ho                                                                              benzimidazol-2-                                                                           0 0 adamantan-1-yl                                                                           H                                                     ylmethylaminocarbonyl                                                                         aminocarbonyl                                               499hp                                                                              benzimidazol-2-                                                                           0 0 adamantan-2-yl                                                                           H                                                     ylmethylaminocarbonyl                                                                         aminocarbonyl                                               499hq                                                                              benzimidazol-2-                                                                           0 0 tetrahydroisoquinolin-                                                                   H                                                     ylmethylaminocarbonyl                                                                         2-ylcarbonyl                                                499hr                                                                              N-(benzimidazol-2-                                                                        0 0 H         NHSO.sub.2 (2,4,6-                                    ylmethyl)-N-methyl-      trimethylphenyl)                                      aminocarbonyl                                                              499hs                                                                              N-(benzimidazol-2-                                                                        0 0 H         NHSO.sub.2 (2,4,6-                                    ylmethyl)-N-methyl-      trichlorophenyl)                                      aminocarbonyl                                                              499ht                                                                              N-(benzimidazol-2-                                                                        0 0 H         NHSO.sub.2 (2,6-                                      ylmethyl)-N-methyl-      dichlorophenyl)                                       aminocarbonyl                                                              499hu                                                                              N-(benzimidazol-2-                                                                        0 0 H         NHSO.sub.2 (2-chloro-6-                               ylmethyl)-N-methyl-      methylphenyl)                                         aminocarbonyl                                                              499hv                                                                              N-(benzimidazol-2-                                                                        0 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)               ylmethyl)-N-methyl-                                                            aminocarbonyl                                                              499hw                                                                              N-(benzimidazol-2-                                                                        0 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                     ylmethyl)-N-methyl-                                                            aminocarbonyl                                                              499hx                                                                              N-(benzimidazol-2-                                                                        0 0 H         NHSO2 4-(2,6-                                         ylmethyl)-N-methyl-      dimethylphenyl)phenyl                                 aminocarbonyl                                                              499hy                                                                              N-(benzimidazol-2-                                                                        0 0 H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                     ylmethyl)-N-methyl-                                                            aminocarbonyl                                                              499hz                                                                              N-(benzimidazol-2-                                                                        0 0 H         NHSO.sub.2  4-(3,5-                                   ylmethyl)-N-methyl-      dimethyl)isoxazolyl!                                  aminocarbonyl                                                              499ia                                                                              N-(benzimidazol-2-                                                                        0 0 H         NHSO.sub.2 (1-napthyl)                                ylmethyl)-N-methyl-                                                            aminocarbonyl                                                              499ib                                                                              N-(benzimidazol-2-                                                                        0 0 H         NHSO.sub.2 (2-napthyl)                                ylmethyl)-N-methyl-                                                            aminocarbonyl                                                              499ic                                                                              N-(benzimidazol-2-                                                                        0 0 H         NHSO.sub.2 NHCH.sub.2 Ph                              ylmethyl)-N-methyl-                                                            aminocarbonyl                                                              499id                                                                              N-(benzimidazol-2-                                                                        0 0 H         NHSO.sub.2 NHPh                                       ylmethyl)-N-methyl-                                                            aminocarbonyl                                                              499ie                                                                              N-(benzimidazol-2-                                                                        0 0 Ph        H                                                     ylmethyl)-N-methyl-                                                            aminocarbonyl                                                              499if                                                                              N-(benzimidazol-2-                                                                        0 0 phenylsulfonylamino                                                                      H                                                     ylmethyl)-N-methyl-                                                                           methyl                                                          aminocarbonyl                                                              499ig                                                                              N-(benzimidazol-2-                                                                        0 0 3-azabicyclo 3.2.2!                                                                      H                                                     ylmethyl)-N-methyl-                                                                           nonan-3-ylcarbonyl                                              aminocarbonyl                                                              499ih                                                                              N-(benzimidazol-2-                                                                        0 0 adamantan-1-yl                                                                           H                                                     ylmethyl)-N-methyl-                                                                           methylaminocarbonyl                                             aminocarbonyl                                                              499ii                                                                              N-(benzimidazol-2-                                                                        0 0 adamantan-1-yl                                                                           H                                                     ylmethyl)-N-methyl-                                                                           aminocarbonyl                                                   aminocarbonyl                                                              499ij                                                                              N-(benzimidazol-2-                                                                        0 0 adamantan-2-yl                                                                           H                                                     ylmethyl)-N-methyl-                                                                           aminocarbonyl                                                   aminocarbonyl                                                              499ik                                                                              N-benzimidazol-2-                                                                         0 0 tetrahydroisoquinolin-                                                                   H                                                     ylmethyl)-N-methyl-                                                                           2-ylcarbonyl                                                    aminocarbonyl                                                              __________________________________________________________________________

                                      TABLE 2                                      __________________________________________________________________________      ##STR35##                                                                     Ex.                                                                            No. R.sup.1 U  m n R.sup.8    R.sup.9     MS                                   __________________________________________________________________________     501 tetrahydropyrimidin-                                                                      3 1 H          H                                                    2-ylamino                                                                  502 tetrahydropyrimidin-                                                                      3 1 H          NHCbz                                                2-ylamino                                                                  503 tetrahydropyrimidin-                                                                      3 1 H          NHtBOC                                               2-ylamino                                                                  504 tetrahydropyrimidin-                                                                      3 1 H          NHCO.sub.2 -nBu                                      2-ylamino                                                                  505 tetrahydropyrimidin-                                                                      3 1 H          NHCO.sub.2 Et                                        2-ylamino                                                                  506 tetrahydropyrimidin-                                                                      3 1 H          NHCO.sub.2 Me                                        2-ylamino                                                                  507 tetrahydropyrimidin-                                                                      3 1 H          NHCO(CH.sub.2).sub.n Ph                              2-ylamino                                                                  508 tetrahydropyrimidin-                                                                      3 1 H          NHCOtBu                                              2-ylamino                                                                  509 tetrahydropyrimidin-                                                                      3 1 H          NHCO-n-C.sub.5 H.sub.11                              2-ylamino                                                                  510 tetrahydropyrimidin-                                                                      3 1 H          NHCO-n-C.sub.4 H.sub.9                               2-ylamino                                                                  511 tetrahydropyrimidin-                                                                      3 1 H          NHCOCH.sub.2 CH.sub.3                                2-ylamino                                                                  512 tetrahydropyrimidin-                                                                      3 1 H          NHCOCH.sub.3                                         2-ylamino                                                                  513 tetrahydropyrimidin-                                                                      3 1 H          NHSO.sub.2 CH.sub.3                                  2-ylamino                                                                  514 tetrahydropyrimidin-                                                                      3 1 H          NHSO.sub.2 CH.sub.2 CH.sub.3                         2-ylamino                                                                  515 tetrahydropyrimidin-                                                                      3 1 H          NHSO.sub.2 n-Bu                                      2-ylamino                                                                  516 tetrahydropyrimidin-                                                                      3 1 H          NHSO.sub.2 Ph                                        2-ylamino                                                                  517 tetrahydropyrimidin-                                                                      3 1 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-CH.sub.3)              2-ylamino                                                                  518 tetrahydropyrimidin-                                                                      3 1 H          NHSO.sub.2 Bn                                        2-ylamino                                                                  519 tetrahydropyrimidin-                                                                      3 1 H          NHCO(2-pyridyl)                                      2-ylamino                                                                  520 tetrahydropyrimidin-                                                                      3 1 H          NHCO(3-pyridyl)                                      2-ylamino                                                                  521 tetrahydropyrimidin-                                                                      3 1 H          NHCO(4-pyridyl)                                      2-ylamino                                                                  522 tetrahydropyrimidin-                                                                      3 1 H          NHCOCH.sub.2 (2-pyridyl)                             2-ylamino                                                                  523 tetrahydropyrimidin-                                                                      3 1 H          NHCOCH.sub.2 (3-pyridyl)                             2-ylamino                                                                  524 tetrahydropyrimidin-                                                                      3 1 H          NHCOCH.sub.2 (4-pyridyl)                             2-ylamino                                                                  525 tetrahydropyrimidin-                                                                      3 1 H          NHCO.sub.2 CH.sub.2 (2-pyridyl)                      2-ylamino                                                                  526 tetrahydropyrimidin-                                                                      3 1 H          NHCO.sub.2 CH.sub.2 (3-pyridyl)                      2-ylamino                                                                  527 tetrahydropyrimidin-                                                                      3 1 H          NHCO.sub.2 CH.sub.2 (4-pyridyl)                      2-ylamino                                                                  528 imidazolin-2-                                                                             3 1 H          H                                                    ylamino                                                                    529 imidazolin-2-                                                                             3 1 H          NHCbz                                                ylamino                                                                    530 imidazolin-2-                                                                             3 1 H          NHtBOC                                               ylamino                                                                    531 imidazolin-2-                                                                             3 1 H          NHCO.sub.2 -nBu                                      ylamino                                                                    532 imidazolin-2-                                                                             3 1 H          NHCO.sub.2 Et                                        ylamino                                                                    533 imidazolin-2-                                                                             3 1 H          NHCO.sub.2 Me                                        ylamino                                                                    534 imidazolin-2-                                                                             3 1 H          NHCO(CH.sub.2).sub.n Ph                              ylamino                                                                    535 imidazolin-2-                                                                             3 1 H          NHCOtBu                                              ylamino                                                                    536 imidazolin-2-                                                                             3 1 H          NHCO-n-C.sub.5 H.sub.11                              ylamino                                                                    537 imidazolin-2-                                                                             3 1 H          NHCO-n-C.sub.4 H.sub.9                               ylamino                                                                    538 imidazolin-2-                                                                             3 1 H          NHCOCH.sub.2 CH.sub.3                                ylamino                                                                    539 imidazolin-2-                                                                             3 1 H          NHCOCH.sub.3                                         ylamino                                                                    540 imidazolin-2-                                                                             3 1 H          NHSO.sub.2 CH.sub.3                                  ylamino                                                                    541 imidazolin-2-                                                                             3 1 H          NHSO.sub.2 CH.sub.2 CH.sub.3                         ylamino                                                                    542 imidazolin-2-                                                                             3 1 H          NHSO.sub.2 n-Bu                                      ylamino                                                                    543 imidazolin-2-                                                                             3 1 H          NHSO.sub.2 Ph                                        ylamino                                                                    544 imidazolin-2-                                                                             3 1 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-CH.sub.3)              ylamino                                                                    545 imidazolin-2-                                                                             3 1 H          NHSO.sub.2 Bn                                        ylamino                                                                    546 imidazolin-2-                                                                             3 1 H          NHCO(2-pyridyl)                                      ylamino                                                                    547 imidazolin-2-                                                                             3 1 H          NHCO(3-pyridyl)                                      ylamino                                                                    548 imidazolin-2-                                                                             3 1 H          NHCO(4-pyridyl)                                      ylamino                                                                    549 imidazolin-2-                                                                             3 1 H          NHCOCH.sub.2 (2-pyridyl)                             ylamino                                                                    550 imidazolin-2-                                                                             3 1 H          NHCOCH.sub.2 (3-pyridyl)                             ylamino                                                                    551 imidazolin-2-                                                                             3 1 H          NHCOCH.sub.2 (4-pyridyl)                             ylamino                                                                    552 imidazolin-2-                                                                             3 1 H          NHCO.sub.2 CH.sub.2 (2-pyridyl)                      ylamino                                                                    553 imidazolin-2-                                                                             3 1 H          NHCO.sub.2 CH.sub.2 (3-pyridyl)                      ylamino                                                                    554 imidazolin-2-                                                                             3 1 H          NHCO.sub.2 CH.sub.2 (4-pyridyl)                      ylamino                                                                    555 tetrahydropyrimidin-                                                                      4 0 H          H                                                    2-ylamino                                                                  556 tetrahydropyrimidin-                                                                      4 0 H          NHCbz                                                2-ylamino                                                                  557 tetrahydropyrimidin-                                                                      4 0 H          NHtBOC                                               2-ylamino                                                                  558 tetrahydropyrimidin-                                                                      4 0 H          NHCO.sub.2 -nBu                                      2-ylamino                                                                  559 tetrahydropyrimidin-                                                                      4 0 H          NHCO.sub.2 Et                                        2-ylamino                                                                  560 tetrahydropyrimidin-                                                                      4 0 H          NHCO.sub.2 Me                                        2-ylamino                                                                  561 tetrahydropyrimidin-                                                                      4 0 H          NHCO(CH.sub.2).sub.n Ph                              2-ylamino                                                                  562 tetrahydropyrimidin-                                                                      4 0 H          NHCOtBu                                              2-ylamino                                                                  563 tetrahydropyrimidin-                                                                      4 0 H          NHCO-n-C.sub.5 H.sub.11                              2-ylamino                                                                  564 tetrahydropyrimidin-                                                                      4 0 H          NHCO-n-C.sub.4 H.sub.9                               2-ylamino                                                                  565 tetrahydropyrimidin-                                                                      4 0 H          NHCOCH.sub.2 CH.sub.3                                2-ylamino                                                                  566 tetrahydropyrimidin-                                                                      4 0 H          NHCOCH.sub.3                                         2-ylamino                                                                  567 tetrahydropyrimidin-                                                                      4 0 H          NHSO.sub.2 CH.sub.3                                  2-ylamino                                                                  568 tetrahydropyrimidin-                                                                      4 0 H          NHSO.sub.2 CH.sub.2 CH.sub.3                         2-ylamino                                                                  569 tetrahydropyrimidin-                                                                      4 0 H          NHSO.sub.2 n-Bu                                      2-ylamino                                                                  570 tetrahydropyrimidin-                                                                      4 0 H          NHSO.sub.2 Ph                                        2-ylamino                                                                  571 tetrahydropyrimidin                                                                       4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-CH.sub.3)              2-ylamino                                                                  572 tetrahydropyrimidin                                                                       4 0 H          NHSO.sub.2 Bn                                        2-ylamino                                                                  573 tetrahydropyrimidin                                                                       4 0 H          NHCO(2-pyridyl)                                      2-ylamino                                                                  574 tetrahydropyrimidin                                                                       4 0 H          NHCO(3-pyridyl)                                      2-ylamino                                                                  575 tetrahydropyrimidin                                                                       4 0 H          NHCO(4-pyridyl)                                      2-ylamino                                                                  576 tetrahydropyrimidin                                                                       4 0 H          NHCOCH.sub.2 (2-pyridyl)                             2-ylamino                                                                  577 tetrahydropyrimidin-                                                                      4 0 H          NHCOCH.sub.2 (3-pyridyl)                             2-ylamino                                                                  578 tetrahydropyrimidin-                                                                      4 0 H          NHCOCH.sub.2 (4-pyridyl)                             2-ylamino                                                                  579 tetrahydropyrimidin                                                                       4 0 H          NHCO.sub.2 CH.sub.2 (2-pyridyl)                      2-ylamino                                                                  580 tetrahydropyrimidin                                                                       4 0 H          NHCO.sub.2 CH.sub.2 (3-pyridyl)                      2-ylamino                                                                  581 tetrahydropyrimidin                                                                       4 0 H          NHCO.sub.2 CH.sub.2 (4-pyridyl)                      2-ylamino                                                                  582 imidazolin-2-                                                                             4 0 H          H                                                    ylamino                                                                    583 imidazolin-2-                                                                             4 0 H          NHCbz       475.4                                    ylamino                                                                    584 imidazolin-2-                                                                             4 0 H          NHtBOC                                               ylamino                                                                    585 imidazolin-2-                                                                             4 0 H          NHCO.sub.2 -nBu                                      ylamino                                                                    586 imidazolin-2-                                                                             4 0 H          NHCO.sub.2 Et                                        ylamino                                                                    587 imidazolin-2-                                                                             4 0 H          NHCO.sub.2 Me                                        ylamino                                                                    588 imidazolin-2-                                                                             4 0 H          NHCO(CH.sub.2).sub.n Ph                              ylamino                                                                    589 imidazolin-2-                                                                             4 0 H          NHCOtBu                                              ylamino                                                                    590 imidazolin-2-                                                                             4 0 H          NHCO-n-C.sub.5 H.sub.11                              ylamino                                                                    591 imidazolin-2-                                                                             4 0 H          NHCO-n-C.sub.4 H.sub.9                               ylamino                                                                    592 imidazolin-2-                                                                             4 0 H          NHCOCH.sub.2 CH.sub.3                                ylamino                                                                    593 imidazolin-2-                                                                             4 0 H          NHCOCH.sub.3                                         ylamino                                                                    594 imidazolin-2-                                                                             4 0 H          NHSO.sub.2 CH.sub.3                                  ylamino                                                                    595 imidazolin-2-                                                                             4 0 H          NHSO.sub.2 CH.sub.2 CH.sub.3                         ylamino                                                                    596 imidazolin-2-                                                                             4 0 H          NHSO.sub.2 n-Bu                                      ylamino                                                                    597 imidazolin-2-                                                                             4 0 H          NHSO.sub.2 Ph                                                                              481.3                                    ylamino                                                                    598 imidazolin-2-                                                                             4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-CH.sub.3)              ylamino                                                                    599 imidazolin-2-                                                                             4 0 H          NHSO.sub.2 Bn                                        ylamino                                                                    600 imidazolin-2-                                                                             4 0 H          NHCO(2-pyridyl)                                      ylamino                                                                    601 imidazolin-2-                                                                             4 0 H          NHCO(3-pyridyl)                                      ylamino                                                                    602 imidazolin-2-                                                                             4 0 H          NHCO(4-pyridyl)                                      ylamino                                                                    603 imidazolin-2-                                                                             4 0 H          NHCOCH.sub.2 (2-pyridyl)                             ylamino                                                                    604 imidazolin-2-                                                                             4 0 H          NHCOCH.sub.2 (3-pyridyl)                             ylamino                                                                    605 imidazolin-2-                                                                             4 0 H          NHCOCH.sub.2 (4-pyridyl)                             ylamino                                                                    606 imidazolin-2-                                                                             4 0 H          NHCO.sub.2 CH.sub.2 (2-pyridyl)                      ylamino                                                                    607 imidazolin-2-                                                                             4 0 H          NHCO.sub.2 CH.sub.2 (3-pyridyl)                      ylamino                                                                    608 imidazolin-2-                                                                             4 0 H          NHCO.sub.2 CH.sub.2 (4-pyridyl)                      ylamino                                                                    609 tetrahydropyrimidin-                                                                      3 0 H          H                                                    2-ylamino                                                                  610 tetrahydropyrimidin-                                                                      3 0 H          NHCbz                                                2-ylamino                                                                  611 tetrahydropyrimidin-                                                                      3 0 H          NHtBOC                                               2-ylamino                                                                  612 tetrahydropyrimidin                                                                       3 0 H          NHCO.sub.2 -nBu                                      2-ylamino                                                                  613 tetrahydropyrimidin-                                                                      3 0 H          NHCO.sub.2 Et                                        2-ylamino                                                                  614 tetrahydropyrimidin-                                                                      3 0 H          NHCO.sub.2 Me                                        2-ylamino                                                                  615 tetrahydropyrimidin-                                                                      3 0 H          NHCO(CH.sub.2).sub.n Ph                              2-ylamino                                                                  616 tetrahydropyrimidin-                                                                      3 0 H          NHCOtBu                                              2-ylamino                                                                  617 tetrahydropyrimidin-                                                                      3 0 H          NHCO-n-C.sub.5 H.sub.11                              2-ylamino                                                                  618 tetrahydropyrimidin-                                                                      3 0 H          NHCO-n-C.sub.4 H.sub.9                               2-ylamino                                                                  619 tetrahydropyrimidin-                                                                      3 0 H          NHCOCH.sub.2 CH.sub.3                                2-ylamino                                                                  620 tetrahydropyrimidin-                                                                      3 0 H          NHCOCH.sub.3                                         2-ylamino                                                                  621 tetrahydropyrimidin-                                                                      3 0 H          NHSO.sub.2 CH.sub.3                                  2-ylamino                                                                  622 tetrahydropyrimidin-                                                                      3 0 H          NHSO.sub.2 CH.sub.2 CH.sub.3                         2-ylamino                                                                  623 tetrahydropyrimidin-                                                                      3 0 H          NHSO.sub.2 n-Bu                                      2-ylamino                                                                  624 tetrahydropyrimidin-                                                                      3 0 H          NHSO.sub.2 Ph                                        2-ylamino                                                                  625 tetrahydropyrimidin-                                                                      3 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-CH.sub.3)              2-ylamino                                                                  626 tetrahydropyrimidin-                                                                      3 0 H          NHSO.sub.2 Bn                                        2-ylamino                                                                  627 tetrahydropyrimidin-                                                                      3 0 H          NHCO(2-pyridyl)                                      2-ylamino                                                                  628 tetrahydropyrimidin-                                                                      3 0 H          NHCO(3-pyridyl)                                      2-ylamino                                                                  629 tetrahydropyrimidin-                                                                      3 0 H          NHCO(4-pyridyl)                                      2-ylamino                                                                  630 tetrahydropyrimidin-                                                                      3 0 H          NHCOCH.sub.2 (2-pyridyl)                             2-ylamino                                                                  631 tetrahydropyrimidin-                                                                      3 0 H          NHCOCH.sub.2 (3-pyridyl)                             2-ylamino                                                                  632 tetrahydropyrimidin-                                                                      3 0 H          NHCOCH.sub.2 (4-pyridyl)                             2-ylamino                                                                  633 tetrahydropyrimidin-                                                                      3 0 H          NHCO.sub.2 CH.sub.2 (2-pyridyl)                      2-ylamino                                                                  634 tetrahydropyrimidin-                                                                      3 0 H          NHCO.sub.2 CH.sub.2 (3-pyridyl)                      2-ylamino                                                                  635 tetrahydropyrimidin-                                                                      3 0 H          NHCO.sub.2 CH.sub.2 (4-pyridyl)                      2-ylamino                                                                  636 imidazolin-2-                                                                             3 0 H          H                                                    ylamino                                                                    637 imidazolin-2-                                                                             3 0 H          NHCbz       461.3                                    ylamino                                                                    638 imidazolin-2-                                                                             3 0 H          NHtBOC                                               ylamino                                                                    639 imidazolin-2-                                                                             3 0 H          NHCO.sub.2 -nBu                                      ylamino                                                                    640 imidazolin-2-                                                                             3 0 H          NHCO.sub.2 Et                                        ylamino                                                                    641 imidazolin-2-                                                                             3 0 H          NHCO.sub.2 Me                                        ylamino                                                                    642 imidazolin-2-                                                                             3 0 H          NHCO(CH.sub.2).sub.n Ph                              ylamino                                                                    643 imidazolin-2-                                                                             3 0 H          NHCOtBu                                              ylamino                                                                    644 imidazolin-2-                                                                             3 0 H          NHCO-n-C.sub.5 H.sub.11                              ylamino                                                                    645 imidazolin-2-                                                                             3 0 H          NHCO-n-C.sub.4 H.sub.9                               ylamino                                                                    646 imidazolin-2-                                                                             3 0 H          NHCOCH.sub.2 CH.sub.3                                ylamino                                                                    647 imidazolin-2-                                                                             3 0 H          NHCOCH.sub.3                                         ylamino                                                                    648 imidazolin-2-                                                                             3 0 H          NHSO.sub.2 CH.sub.3                                  ylamino                                                                    649 imidazolin-2-                                                                             3 0 H          NHSO.sub.2 CH.sub.2 CH.sub.3                         ylamino                                                                    650 imidazolin-2-                                                                             3 0 H          NHSO.sub.2 n-Bu                                      ylamino                                                                    651 imidazolin-2-                                                                             3 0 H          NHSO.sub.2 Ph                                        ylamino                                                                    652 imidazolin-2-                                                                             3 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-CH.sub.3)              ylamino                                                                    653 imidazolin-2-                                                                             3 0 H          NHSO.sub.2 Bn                                        ylamino                                                                    654 imidazolin-2-                                                                             3 0 H          NHCO(2-pyridyl)                                      ylamino                                                                    655 imidazolin-2-                                                                             3 0 H          NHCO(3-pyridyl)                                      ylamino                                                                    656 imidazolin-2-                                                                             3 0 H          NHCO(4-pyridyl)                                      ylamino                                                                    657 imidazolin-2-                                                                             3 0 H          NHCOCH.sub.2 (2-pyridyl)                             ylamino                                                                    658 imidazolin-2-                                                                             3 0 H          NHCOCH.sub.2 (3-pyridyl)                             ylamino                                                                    659 imidazolin-2-                                                                             3 0 H          NHCOCH.sub.2 (4-pyridyl)                             ylamino                                                                    660 imidazolin-.2-                                                                            3 0 H          NHCO.sub.2 CH.sub.2 (2-pyridyl)                      ylamino                                                                    661 imidazolin-2-                                                                             3 0 H          NHCO.sub.2 CH.sub.2 (3-pyridyl)                      ylamino                                                                    662 imidazolin-2-                                                                             3 0 H          NHCO.sub.2 CH.sub.2 (4-pyridyl)                      ylamino                                                                    663 pyridin-2-ylamino                                                                         3 1 H          NHCbz                                            664 pyridin-2-ylamino                                                                         3 1 H          NHCO.sub.2 -n-Bu                                 665 pyridin-2-ylamino                                                                         3 1 H          NHSO.sub.2 Ph                                    666 pyridin-2-ylamino                                                                         3 1 H          NHSO.sub.2 -nBu                                  667 pyridin-2-ylamino                                                                         4 0 H          NHCbz       484.3                                668 pyridin-2-ylamino                                                                         4 0 H          NHCO.sub.2 -n-Bu                                 669 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 Ph                                                                              490.2                                670 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 -nBu                                  671 pyridin-2-ylamino                                                                         3 0 H          NHCbz                                            672 pyridin-2-ylamino                                                                         3 0 H          NHCO.sub.2 -n-Bu                                 673 pyridin-2-ylamino                                                                         3 0 H          NHSO.sub.2 Ph                                    674 pyridin-2-ylamino                                                                         3 0 H          NHSO.sub.2 -nBu                                  675 imidazol-2-ylamino                                                                        3 1 H          NHCbz                                            676 imidazol-2-ylamino                                                                        3 1 H          NHCO.sub.2 -n-Bu                                 677 imidazol-2-ylamino                                                                        3 1 H          NHSO.sub.2 Ph                                    678 imidazol-2-ylamino                                                                        3 1 H          NHSO.sub.2 -nBu                                  679 imidazol-2-ylamino                                                                        4 0 H          NHCbz                                            680 imidazol-2-ylamino                                                                        4 0 H          NHCO.sub.2 -n-Bu                                 681 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 Ph                                    682 imidazol-2-ylamino                                                                        4.                                                                               0 H          NHSO.sub.2 -nBu                                  683 imidazol-2-ylamino                                                                        3 0 H          NHCbz                                            684 imidazol-2-ylamino                                                                        3 0 H          NHCO.sub.2 -n-Bu                                 685 imidazol-2-ylamino                                                                        3 0 H          NHSO.sub.2 Ph                                    686 imidazol-2-ylamino                                                                        3 0 H          NHSO.sub.2 -nBu                                  687 thiazol-2-ylamino                                                                         3 1 H          NHCbz                                            688 2-aminopyridin-6-yl                                                                       3 1 H          NHCO.sub.2 -n-Bu                                 689 2-aminopyridin-6-yl                                                                       3 1 H          NHSO.sub.2 Ph                                    690 2-aminopyridin-6-yl                                                                       3 1 H          NHSO.sub.2 -nBu                                  691 2-aminopyridin-6-yl                                                                       4 0 H          NHCbz                                            692 2-aminopyridin-6-yl                                                                       4 0 H          NHCO.sub.2 -n-Bu                                 693 2-aminopyridin-6-yl                                                                       4 0 H          NHSO.sub.2 Ph                                    694 2-aminopyridin-6-yl                                                                       4 0 H          NHSO.sub.2 -nBu                                  695 2-aminopyridin-6-yl                                                                       3 0 H          NHCbz       470.5                                696 2-aminopyridin-6-yl                                                                       3 0 H          NHCO.sub.2 -n-Bu                                 697 2-aminopyridin-6-yl                                                                       3 0 H          NHSO.sub.2 Ph                                                                              476.4                                698 2-aminopyridin-6-yl                                                                       3 0 H          NHSO.sub.2 -nBu                                  699 2-aminopyridin-3-yl                                                                       2 0 H          NHCbz                                            700 2-aminopyridin-3-yl                                                                       2 0 H          NHCO.sub.2 -n-Bu                                 701 2-aminopyridin-3-yl                                                                       2 0 H          NHSO.sub.2 Ph                                    702 2-aminopyridin-3-yl                                                                       2 0 H          NHSO.sub.2 -nBu                                  703 2-aminothiazol-4-yl                                                                       3 1 H          NHCbz                                            704 2-aminothiazol-4-yl                                                                       3 1 H          NHCO.sub.2 -n-Bu                                 705 2-aminothiazol-4-yl                                                                       3 1 H          NHSO.sub.2 Ph                                    706 2-aminothiazol-4-yl                                                                       3 1 H          NHSO.sub.2 -nBu                                  707 2-aminothiazol-4-yl                                                                       4 0 H          NHCbz                                            708 2-aminothiazol-4-yl                                                                       4 0 H          NHCO.sub.2 -n-Bu                                 709 2-aminothiazol-4-yl                                                                       4 0 H          NHSO.sub.2 Ph                                    710 2-aminopyridin-6-yl                                                                       4 0 H          NHSO.sub.2 -nBu                                  711 2-aminothiazol-4-yl                                                                       3 0 H          NHCbz                                            712 2-aminothiazol-4-yl                                                                       3 0 H          NHCO.sub.2 -n-Bu                                 713 2-aminothiazol-4-yl                                                                       3 0 H          NHSO.sub.2 Ph                                    714 2-aminothiazol-4-yl                                                                       3 0 H          NHSO.sub.2 -nBu                                  715 2-aminothiazol-4-yl                                                                       3 1 H          NHCbz                                            716 2-aminothiazol-4-yl                                                                       3 1 H          NHCO.sub.2 -n-Bu                                 775 imidazolin-2-                                                                             2 2 H          NHCbz                                                ylamino                                                                    776 imidazolin-2-                                                                             2 2 H          NHCO.sub.2 -n-Bu                                     ylamino                                                                    777 imidazolin-2-                                                                             2 2 H          NHSO.sub.2 Ph                                        ylamino                                                                    778 imidazolin-2-                                                                             2 2 H          NHSO.sub.2 -nBu                                      ylamino                                                                    779 tetrahydropyrimidin-                                                                      2 2 H          NHCbz                                                2-ylamino                                                                  780 tetrahydropyrimidin-                                                                      2 2 H          NHCO.sub.2 -n-Bu                                     2-ylamino                                                                  781 tetrahydropyrimidin-                                                                      2 2 H          NHSO.sub.2 Ph                                        2-ylamino                                                                  782 tetrahydropyrimidin-                                                                      2 2 H          NHSO.sub.2 -nBu                                      2-ylamino                                                                  783 benzimidazol-2-                                                                           4 0 H          NHCbz                                                ylamino                                                                    784 benzthiazol-2-                                                                            4 0 H          NHCbz                                                ylamino                                                                    787 imidazol-4-ylamino                                                                        4 0 H          NHCbz                                            794 2-iminopyrrolidin-                                                                        3 1 H          NHCbz                                                5-yl                                                                       795 2-iminopyrrolidin-                                                                        3 1 H          NHSO.sub.2 Ph                                        5-yl                                                                       796 2-iminopyrrolidin-                                                                        3 0 H          NHCbz                                                5-yl                                                                       797 2-iminopyrrolidin-                                                                        3 0 H          NHSO.sub.2 Ph                                        5-yl                                                                       798 2-iminopyrrolidin-                                                                        2 1 H          NHCbz                                                5-yl                                                                       799 2-iminopyrrolidin-                                                                        2 1 H          NHSO.sub.2 Ph                                        5-yl                                                                       800 2-iminopiperidin-6-                                                                       3 1 H          NHCbz                                                yl                                                                         801 2-iminopiperidin-6-                                                                       3 1 H          NHSO.sub.2 Ph                                        yl                                                                         802 2-iminopiperidin-6-                                                                       3 0 H          NHCbz                                                yl                                                                         803 2-iminopiperidin-6-                                                                       3 0 H          NHSO.sub.2 Ph                                        yl                                                                         804 2-iminopiperidin-6-                                                                       2 1 H          NHCbz                                                yl                                                                         805 2-iminopiperidin-6-                                                                       2 1 H          NHSO.sub.2 Ph                                        yl                                                                         806 2-iminoazepin-7-yl                                                                        3 1 H          NHCbz                                            807 2-iminoazepin-7-yl                                                                        3 1 H          NHSO.sub.2 Ph                                    808 2-iminoazepin-7-yl                                                                        3 0 H          NHCbz                                            809 2-iminoazepin-7-yl                                                                        3 0 H          NHSO.sub.2 Ph                                    810 2-iminoazepin-7-yl                                                                        2 1 H          NHCbz                                            811 2-iminoazepin-7-yl                                                                        2 1 H          NHSO.sub.2 Ph                                    812 benzimidazol-2-                                                                           4 0 n-Bu       H                                                    ylamino                                                                    813 benzthiazol-2-                                                                            4 0 n-Bu       H                                                    ylamino                                                                    816 imidazol-4-ylamino                                                                        4 0 n-Bu       H                                                823 imidazolin-2-                                                                             2 0 H          NHCbz       447.4                                    ylamino                                                                    824 imidazolin-2-                                                                             2 0 H          NHSO2Ph                                              ylamino                                                                    830 pyridin-2-ylamino                                                                         4 0 H          N(Me)SO.sub.2 C.sub.6 H.sub.4 -(3-Me)                                                      518.2                                831 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(2-Me)                                                         504.3                                832 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(3-Me)                                                         504.2                                833 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-Me)                                                         504.2                                834 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(2-Br)                                                         568.1                                835 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(3-Br)                                                         570.0                                836 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-Br)                                                         570.0                                837 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(2-F)                                                          508.2                                838 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-F)                                                          508.2                                839 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(2-CF.sub.3)                                                   558.3                                840 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(3-CF.sub.3)                                                   558.1                                841 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-CF.sub.3)         842 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-OCH.sub.3)                                                  520.1                                843 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-CN)                                                         515.2                                844 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2  4-                                                                             547.3                                                              (acetylamino)phenyl!                             845 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-OCF.sub.3)                                                  574.3                                846 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-                                                            532.4                                                              isopropyl)                                       847 pyridin-2-ylamino                                                                         4 0 H          NHSO2(2,6-  558.3                                                              dichlorophenyl)                                  848 pyridin-2-ylamino                                                                         4 0 H          NHSO2(2-chloro-6-                                                                          538.3                                                              methylphenyl)                                    849 pyridin-2-ylamino                                                                         4 0 H          NHSO2(2,4,6-                                                                               532.2                                                              trimethylphenyl)                                 850 pyridin-2-ylamino                                                                         4 0 H          NHSO2(2,4,6-                                                                               616.4                                                              triisopropylphenyl)                              851 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-Ph)                                                         566.1                                852 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2  4-(2,6-                                                            dimethylphenyl)phenyl                            853 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 (1-napthyl)                                                                     540.1                                854 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 (2-napthyl)                                                                     540.3                                855 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 (8-quinolinyl)                                                                  541.1                                856 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2(CHCH)C.sub.6 H.sub.5                                                            516.1                                857 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 CH.sub.2 Ph                                                                     504.3                                858 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 (2-thienyl)                                                                     496.1                                859 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2  2-(5-                                                                          530.2                                                              chloro)thienyl!                                  860 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2  2-(5-pyridin-2-                                                                573.0                                                              yl)thienyl!                                      861 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2  3-(2-                                                                          554.1                                                              (methoxycarbonyl)                                                              thienyl!                                         862 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2  2-(5-isoxazol-3-                                                               563.3                                                              yl)thienyl!                                      863 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2  2-(4-                                                                          636.1                                                              phenylsulfonyl)                                                                thienyl!                                         864 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2  3-(2-(1-CH.sub.3 -5-                                                           644.0                                                              CF.sub.3 -pyrazol-3-yl))                                                       thienyl!                                         865 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2  2-(5-(5-CF.sub.3 -                                                             705.2                                                              pyridine-2-                                                                    yl)sulfonyl)thienyl!                             866 pyridin-2-ylamino                                                                         4 0 H          NHSO2 2-(5-(5-CF3-3-                                                                       739.2                                                              chloropyridine-2-                                                              yl)sulfonyl)thienyl!                             867 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2  2-(4,5-                                                                        564.2                                                              dichloro)thienyl!                                868 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2  2-(3-bromo-5-                                                                  610.0                                                              chloro)thienyl!                                  869 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2  3-(2,5-                                                                        564.0                                                              dichloro)thienyl!                                870 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2  4-(1-                                                                          494.1                                                              methyl)imidazolyl!                               871 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2  4-(1,3-dimethyl-                                                               542.1                                                              5-chloro)pyrazolyl!                              872 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2  4-(3,5-                                                                        509.2                                                              dimethyl)isoxazolyl!                             873 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 NH(cyclohexyl)                        874 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 NHCH2Ph                               875 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 NHPh                                  876 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 NH(2,6-dichloro)                                                    Ph                                               877 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 NH(2,6-dimethoxy)                                                   Ph                                               878 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 NH(2,4,6-                                                           trimethyl)Ph                                     879 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 NH(4-Ph)Ph                            880 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 NH(1-napthyl)                         881 pyridin-2-ylamino                                                                         4 0 H          NHSO.sub.2 NH(2-napthyl)                         882 pyridin-2-ylamino                                                                         4 0 Et         H                                                883 pyridin-2-ylamino                                                                         4 0 Ph         H                                                884 pyridin-2-ylamino                                                                         4 0 3-pyridyl  H           412.2                                885 pyridin-2-ylamino                                                                         4 0 CH.sub.2 Ph                                                                               H                                                886 pyridin-2-ylamino                                                                         4 0 phenylsulfonylamino                                                                       H                                                                   methyl                                                      887 pyridin-2-ylamino                                                                         4 0 3-azabicyclo 3.2.2!                                                                       H                                                                   nonan-3-ylcarbonyl                                          888 pyridin-2-ylamino                                                                         4 0 adamantan-1-yl                                                                            H                                                                   methylaminocarbonyl                                         889 pyridin-2-ylamino                                                                         4 0 adamantan-2-yl                                                                            H                                                                   aminocarbonyl                                               890 pyridin-2-ylamino                                                                         4 0 tetrahydroisoquinol                                                                       H                                                                   in-2-ylcarbonyl                                             891 pyridin-2-ylamino                                                                         4 0 phenylethylaminocar                                                                       H                                                                   bonyl                                                       892 pyridin-2-ylamino                                                                         4 0  N-(phenylethyl)N-                                                                        H                                                                   (methyl)amino!carbonyl                                      893 imidazolin-2-                                                                             4 0 H          NHSO.sub.2 (2,4,6-                                   ylamino                   trimethylphenyl)                                 894 imidazolin-2-                                                                             4 0 H          NHSO.sub.2 (2,4,6-                                   ylamino                   trichlorophenyl)                                 895 imidazolin-2-                                                                             4 0 H          NHSO.sub.2 (2,6-                                     ylamino                   dichlorophenyl)                                  896 imidazolin-2-                                                                             4 0 H          NHSO.sub.2 (2-chloro-6-                              ylamino                   methylphenyl)                                    897 imidazolin-2-                                                                             4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)              ylamino                                                                    898 imidazolin-2-                                                                             4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                    ylamino                                                                    899 imidazolin-2-                                                                             4 0 H          NHSO2 4-(2,6-                                        ylamino                   dimethylphenyl)phenyl                            900 imidazolin-2-                                                                             4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                    ylamino                                                                    901 imidazolin-2-                                                                             4 0 H          NHSO.sub.2  4-(3,5-                                  ylamino                   dimethyl)isoxazolyl!                             902 imidazolin-2-                                                                             4 0 H          NHSO.sub.2 (1-napthyl)                               ylamino                                                                    903 imidazolin-2-                                                                             4 0 H          NHSO.sub.2 (2-napthyl)                               ylamino                                                                    904 imidazolin-2-                                                                             4 0 H          NHSO.sub.2 NHCH.sub.2 Ph                             ylamino                                                                    905 imidazolin-2-                                                                             4 0 H          NHSO.sub.2 NHPh                                      ylamino                                                                    906 imidazolin-2-                                                                             4 0 Ph         H                                                    ylamino                                                                    907 Imidazolin-2-                                                                             4 0 phenylsulfonylamino                                                                       H                                                    ylamino        methyl                                                      908 imidazolin-2-                                                                             4 0 3-azabicyclo 3.2.2!                                                                       H                                                    ylamino        nonan-3-ylcarbonyl                                          909 imidazolin-2-                                                                             4 0 adamantan-1-yl                                                                            H                                                    ylamino        methylaminocarbonyl                                         910 imidazolin-2-                                                                             4 0 adamantan-1-yl                                                                            H                                                    ylamino        aminocarbonyl                                               911 imidazolin-2-                                                                             4 0 adamantan-2-yl                                                                            H                                                    ylamino        aminocarbonyl                                               912 imidazolin-2-                                                                             4 0 tetrahydroisoquinol                                                                       H                                                    ylamino        in-2-ylcarbonyl                                             913 tetrahydropyrimidin-                                                                      4 0 H          NHSO.sub.2 (2,4,6-                                   2-ylamino                 trimethylphenyl)                                 914 tetrahydropyrimidin-                                                                      4 0 H          NHSO.sub.2 (2,4,6-                                   2-ylamino                 trichlorophenyl)                                 915 tetrahydropyrimidin-                                                                      4 0 H          NHSO.sub.2 (2,6-                                     2-ylamino                 dichlorophenyl)                                  916 tetrahydropyrimidin-                                                                      4 0 H          NHSO.sub.2 (2-chloro-6-                              2-ylamino                 methylphenyl)                                    917 tetrahydropyrimidin-                                                                      4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)              2-ylamino                                                                  918 tetrahydropyrimidin-                                                                      4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                    2-ylamino                                                                  919 tetrahydropyrimidin-                                                                      4 0 H          NHSO2 4-(2,6-                                        2-ylamino                 dimethylphenyl)phenyl                            920 tetrahydropyrimidin-                                                                      4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                    2-ylamino                                                                  921 tetrahydropyrimidin-                                                                      4 0 H          NHSO.sub.2  4-(3,5-                                  2-ylamino                 dimethyl)isoxazolyl!                             922 tetrahydropyrimidin-                                                                      4 0 H          NHSO.sub.2 (1-napthyl)                               2-ylamino                                                                  923 tetrahydropyrimidin-                                                                      4 0 H          NHSO.sub.2 (2-napthyl)                               2-ylamino                                                                  924 tetrahydropyrimidin-                                                                      4 0 H          NHSO.sub.2 NHCH.sub.2 Ph                             2-ylamino                                                                  925 tetrahydropyrimidin-                                                                      4 0 H          NHSO.sub.2 NHPh                                      2-ylamino                                                                  926 tetrahydropyrimidin-                                                                      4 0 Ph         H                                                    2-ylamino                                                                  927 tetrahydropyrimidin-                                                                      4 0 phenylsulfonylamino H                                           2-ylamino      methyl                                                      928 tetrahydropyrimidin-                                                                      4 0 3-azabicyclo 3.2.2!                                                                       H                                                    2-ylamino      nonan-3-ylcarbonyl                                          929 tetrahydropyrimidin-                                                                      4 0 adamantan-1-yl                                                                            H                                                    2-ylamino      methylaminocarbonyl                                         930 tetrahydropyrimidin-                                                                      4 0 adamantan-1-yl                                                                            H                                                    2-ylamino      aminocarbonyl                                               931 tetrahydropyrimidin-                                                                      4 0 adamantan-2-yl                                                                            H                                                    2-ylamino      aminocarbonyl                                               932 tetrahydropyrimidin-                                                                      4 0 tetrahydroisoquinol                                                                       H                                                    2-ylamino      in-2-ylcarbonyl                                             933 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(2-Me)               934 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(3-Me)               935 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-Me)               936 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(2-Br)               937 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(3-Br)               938 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-Br)               939 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(2-F)                940 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-F)                941 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(2-CF.sub.3)         942 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(3-CF.sub.3)         943 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-CF.sub.3)         944 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-OCH.sub.3)        945 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-CN)               946 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2  4-                                                                 (acetylamino)phenyl!                             947 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-OCF.sub.3)        948 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-                                                isopropyl)                                       949 imidazol-2-ylamino                                                                        4 0 H          NHSO2(2,6-  547.2                                                              dichlorophenyl)                                  950 imidazol-2-ylamino                                                                        4 0 H          NHSO2(2-chloro-6-                                                                          527.3                                                              methylphenyl)                                    951 imidazol-2-ylamino                                                                        4 0 H          NHSO2(2,4,6-                                                                               521.4                                                              trimethylphenyl)                                 952 imidazol-2-ylamino                                                                        4 0 H          NHSO2(2,4,6-                                                                   triisopropylphenyl)                              953 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(4-Ph)               954 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(3-Ph)               955 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 -(2-Ph)               956 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2  4-(2,6-                                                            dimethylphenyl)phenyl                            957 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 (1-napthyl)                                                                     529.3                                958 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 (2-napthyl)                           959 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 (8-quinolinyl)                        960 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 (CHCH)C.sub.6 H.sub.5                 961 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 CH.sub.2 Ph                           962 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 (2-thienyl)                           963 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2  2-(5-                                                              chloro)thienyl!                                  964 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2  2-(5-pyridin-2-                                                    yl)thienyl!                                      965 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2  3-(2-                                                              (methoxycarbonyl)                                                              thienyl!                                         966 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2  2-(5-isoxazol-3-                                                   yl)thiophenyl!                                   967 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2  2-(4-                                                              phenylsulfonyl)                                                                thienyl!                                         968 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2  3-(2-(1-CH.sub.3 -5-                                               CF.sub.3 -pyrazol-3-yl))                                                       thienyl!                                         969 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2  2-(5-(5-CF.sub.3 -                                                 pyridine-2-                                                                    yl)sulfonyl)thienyl!                             970 imidazol-2-ylamino                                                                        4 0 H          NHSO2 2-(5-(5-CF3-3-                                                           chloropyridine-2-                                                              yl)sulfonyl)thienyl!                             971 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2  2-(4,5-                                                            dichloro) thienyl!                               972 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2  2-(3-bromo-5-                                                      chloro)thienyl!                                  973 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2  3-(2,5-                                                            dichloro)thienyl!                                974 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2  4-(1-                                                              methyl)imidazolyl!                               975 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2  4-(1,3-dimethyl-                                                   5-chloro)pyrazolyl!                              975 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2  4-(3,5-                                                                        498.3                                                              dimethyl)isoxazolyl!                             976 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 NH(cyclohexyl)                        977 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 NHCH2Ph                               978 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 NHPh                                  979 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 NH(2,6-dichloro)                                                    Ph                                               980 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 NH(2,6-dimethoxy)                                                   Ph                                               981 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 NH(2,4,6-                                                           trimethyl)Ph                                     982 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 NH(4-Ph)Ph                            983 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 NH(1-napthyl)                         984 imidazol-2-ylamino                                                                        4 0 H          NHSO.sub.2 H(2-napthyl)                          985 imidazol-2-ylamino                                                                        4 0 Et         H                                                986 imidazol-2-ylamino                                                                        4 0 Ph         H                                                987 imidazol-2-ylamino                                                                        4 0 3-pyridyl  H                                                988 imidazol-2-ylamino                                                                        4 0 CH.sub.2 Ph                                                                               H                                                989 imidazol-2-ylamino                                                                        4 0 phenylsulfonylamino                                                                       H                                                                   methyl                                                      990 imidazol-2-ylamino                                                                        4 0 3-azabicyclo 3.2.2!                                                                       H                                                                   nonan-3-ylcarbonyl                                          991 imidazol-2-ylamino                                                                        4 0 adamantan-1-yl                                                                            H                                                                   methylaminocarbonyl                                         992 imidazol-2-ylamino                                                                        4 0 adamantan-2-yl                                                                            H                                                                   aminocarbonyl                                               993 imidazol-2-ylamino                                                                        4 0 tetrahydroisoquinol                                                                       H                                                                   in-2-ylcarbonyl                                             994 imidazol-2-ylamino                                                                        4 0 phenylethylaminocar                                                                       H                                                                   bonyl                                                       995 imidazol-2-ylamino                                                                        4 0  N-(phenylethyl)N-                                                                        H                                                                   (methyl)amino!carbo                                                            nyl                                                         996 2-aminoimidazol-4-                                                                        3 0 H          NHSO.sub.2 Ph                                        yl                                                                         997 2-aminoimidazol-4-                                                                        3 0 H          NHSO.sub.2 (2,4,6-                                   yl                        trimethylphenyl)                                 998 2-aminoimidazol-4-                                                                        3 0 H          NHSO.sub.2 (2,4,6-                                   yl                        trichlorophenyl)                                 999 2-aminoimidazol-4-                                                                        3 0 H          NHSO.sub.2 (2,6-                                     yl                        dichlorophenyl)                                  999a                                                                               2-aminoimidazol-4-                                                                        3 0 H          NHSO.sub.2 (2-chloro-6-                              yl                        methylphenyl)                                    999b                                                                               2-aminoimidazol-4-                                                                        3 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)              yl                                                                         999c                                                                               2-aminoimidazol-4-                                                                        3 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                    yl                                                                         999d                                                                               2-aminoimidazol-4-                                                                        3 0 H          NHSO2 4-(2,6-                                        yl                        dimethylphenyl!phenyl                            999e                                                                               2-aminoimidazol-4-                                                                        3 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                    yl                                                                         999f                                                                               2-aminoimidazol-4-                                                                        3 0 H          NHSO.sub.2  4-(3,5-                                  yl                        dimethyl)isoxazolyl!                             999g                                                                               2-aminoimidazol-4-                                                                        3 0 H          NHSO.sub.2 (1-napthyl)                               yl                                                                         999h                                                                               2-aminoimidazol-4-                                                                        3 0 H          NHSO.sub.2 (2-napthyl)                               yl                                                                         999i                                                                               2-aminoimidazol-4-                                                                        3 0 H          NHSO.sub.2 NHCH.sub.2 Ph                             yl                                                                         999j                                                                               2-aminoimidazol-4-                                                                        3 0 H          NHSO.sub.2 NHPh                                      yl                                                                         999k                                                                               2-aminoimidazol-4-                                                                        3 0 Ph         H                                                    yl                                                                         999l                                                                               2-aminoimidazol-4-                                                                        3 0 phenylsulfonylamino                                                                       H                                                    yl             methyl                                                      999m                                                                               2-aminoimidazol-4-                                                                        3 0 3-azabicyclo 3.2.2!                                                                       H                                                    yl             nonan-3-ylcarbonyl                                          999n                                                                               2-aminoimidazol-4-                                                                        3 0 adamantan-1-yl                                                                            H                                                    yl             methylaminocarbonyl                                         999o                                                                               2-aminoimidazol-4-                                                                        3 0 adamantan-1-yl                                                                            H                                                    yl             aminocarbonyl                                               999p                                                                               2-aminoimidazol-4-                                                                        3 0 adamantan-2-yl                                                                            H                                                    yl             aminocarbonyl                                               999a                                                                               2-aminoimidazol-4-                                                                        3 0 tetrahydroisoquinol                                                                       H                                                    yl             in-2-ylcarbonyl                                             999r                                                                               benzylimidazol-2-yl                                                                       4 0 H          NHSO.sub.2 Ph                                    999s                                                                               benzylimidazol-2-yl                                                                       4 0 H          NHSO.sub.2 (2,4,6-                                                             trimethylphenyl)                                 999t                                                                               benzylimidazol-2-yl                                                                       4 0 H          NHSO.sub.2 (2,4,6-                                                             trichlorophenyl)                                 999u                                                                               benzylimidazol-2-yl                                                                       4 0 H          NHSO.sub.2 (2,6-                                                               dichlorophenyl)                                  999v                                                                               benzylimidazol-2-yl                                                                       4 0 H          NHSO.sub.2 (2-chloro-6-                                                        methylphenyl)                                    999w                                                                               benzylimidazol-2-yl                                                                       4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)          999x                                                                               benzylimidazol-2-yl                                                                       4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                999y                                                                               benzylimidazol-2-yl                                                                       4 0 H          NHSO2 4-(2,6-                                                                  dimethylphenyl)phenyl                            999z                                                                               benzylimidazol-2-yl                                                                       4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                999aa                                                                              benzylimidazol-2-yl                                                                       4 0 H          NHSO.sub.2  4-(3,5-                                                            dimethyl)isoxazolyl!                             999ab                                                                              benzylimidazol-2-yl                                                                       4 0 H          NHSO.sub.2 (1-napthyl)                           999ac                                                                              benzylimidazol-2-yl                                                                       4 0 H          NHSO.sub.2 (2-napthyl)                           999ad                                                                              benzylimidazol-2-yl                                                                       4 0 H          NHSO.sub.2 NHCH.sub.2 Ph                         999ae                                                                              benzylimidazol-2-yl                                                                       4 0 H          NHSO.sub.2 NHPh                                  999af                                                                              benzylimidazol-2-yl                                                                       4 0 Ph         H                                                999ag                                                                              benzylimidazol-2-yl                                                                       4 0 phenylsulfonylamino                                                                       H                                                                   methyl                                                      999ah                                                                              benzylimidazol-2-yl                                                                       4 0 3-azabicyclo 3.2.2!                                                                       H                                                                   nonan-3-ylcarbonyl                                          999ai                                                                              benzylimidazol-2-yl                                                                       4 0 adamantan-1-yl                                                                            H                                                                   methylaminocarbonyl                                         999aj                                                                              benzylimidazol-2-yl                                                                       4 0 adamantan-1-yl                                                                            H                                                                   aminocarbonyl                                               999ak                                                                              benzylimidazol-2-yl                                                                       4 0 adamantan-2-yl                                                                            H                                                                   aminocarbonyl                                               999al                                                                              benzylimidazol-2-yl                                                                       4 0 tetrahydroisoquinol                                                                       H                                                                   in-2-ylcarbonyl                                             999am                                                                              4-methylimidazol-2-                                                                       4 0 H          NHSO.sub.2 Ph                                        ylamino                                                                    999an                                                                              4-methylimidazol-2-                                                                       4 0 H          NHSO.sub.2 (2,4,6-                                   ylamino                   trimethylphenyl)                                 999ao                                                                              4-methylimidazol-2-                                                                       4 0 H          NHSO.sub.2 (2,4,6-                                   ylamino                   trichlorophenyl)                                 999ap                                                                              4-methylimidazol-2-                                                                       4 0 H          NHSO.sub.2 (2,6-                                     ylamino                   dichlorophenyl)                                  999aq                                                                              4-methylimidazol-2-                                                                       4 0 H          NHSO.sub.2 (2-chloro-6-                              ylamino                   methylphenyl)                                    999ar                                                                              4-methylimidazol-2-                                                                       4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)              ylamino                                                                    999as                                                                              4-methylimidazol-2-                                                                       4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                    ylamino                                                                    999at                                                                              4-methylimidazol-2-                                                                       4 0 H          NHSO2 4-(2,6-                                        ylamino                   dimethylphenyl)phenyl                            999au                                                                              4-methylimidazol-2-                                                                       4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                    ylamino                                                                    999av                                                                              4-metbylimidazol-2-                                                                       4 0 H          NHSO.sub.2 4-(3,5-                                   ylamino                   dimethyl)isoxazolyl!                             999aw                                                                              4-methylimidazol-2-                                                                       4 0 H          NHSO.sub.2 (1-napthyl)                               ylamino                                                                    999ax                                                                              4-methylimidazol-2-                                                                       4 0 H          NHSO.sub.2 (2-napthyl)                               ylamino                                                                    999az                                                                              4-methylimidazol-2-                                                                       4 0 H          NHSO.sub.2 NHCH.sub.2 Ph                             ylamino                                                                    999ba                                                                              4-methylimidazol-2-                                                                       4 0 H          NHSO.sub.2 NHPh                                      ylamino                                                                    999bb                                                                              4-methylimidazol-2-                                                                       4 0 Ph         H                                                    ylamino                                                                    999bc                                                                              4-methylimidazol-2-                                                                       4 0 phenylsulfonylamino                                                                       H                                                    ylamino        methyl                                                      999bd                                                                              4-methylimidazol-2-                                                                       4 0 3-azabicyclo 3.2.2!                                                                       H                                                    ylamino        nonan-3-ylcarbonyl                                          999be                                                                              4-methylimidazol-2-                                                                       4 0 adamantan-1-yl                                                                            H                                                    ylamino        methylaminocarbonyl                                         999bf                                                                              4-methylimidazol-2-                                                                       4 0 adamantan-1-yl                                                                            H                                                    ylamino        aminocarbonyl                                               999bg                                                                              4-methylimidazol-2-                                                                       4 0 adamantan-2-yl                                                                            H                                                    ylamino        aminocarbonyl                                               999bh                                                                              4-methylimidazol-2-                                                                       4 0 tetrahydroisoquinol                                                                       H                                                    ylamino        in-2-ylcarbonyl                                             999bi                                                                              4,5-       4 0 H          NHSO.sub.2 Ph                                        dimethylimidazol-2-                                                            ylamino                                                                    999bj                                                                              4,5-       4 0 H          NHSO.sub.2 (2,4,6-                                   dimethylimidazol-2-       trimethylphenyl)                                     ylamino                                                                    999bk                                                                              4,5-       4 0 H          NHSO.sub.2 (2,4,6-                                   dimethylimidazol-2-       trichlorophenyl)                                     ylamino                                                                    999bl                                                                              4,5-       4 0 H          NHSO.sub.2 (2,6-                                     dimethylimidazol-2-       dichlorophenyl)                                      ylamino                                                                    999bm                                                                              4,5-       4 0 H          NHSO.sub.2 (2-chloro-6-                              dimethylimidazol-2-       methylphenyl)                                        ylamino                                                                    999bn                                                                              4,5-       4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)              dimethylimidazol-2-                                                            ylamino                                                                    999bo                                                                              4,5-       4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                    dimethylimidazol-2-                                                            ylamino                                                                    999bp                                                                              4,5-       4 0 H          NHSO.sub.2  4-(2,6-                                  dimethylimidazol-2-       dimethylphenyl)phenyl                                ylamino                                                                    999bq                                                                              4,5-       4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                    dimethylimidazol-2-                                                            ylamino                                                                    999br                                                                              4,5-       4 0 H          NHSO.sub.2 4-(3,-5-                                  dimethylimidazol-2-       dimethyl)isoxazolyl!                                 ylamino                                                                    999bs                                                                              4,5-       4 0 H          NHSO.sub.2 (1-napthyl)                               dimethylimidazol- 2-                                                           ylamino                                                                    999bt                                                                              4,5-       4 0 H          NHSO.sub.2 (2-napthyl)                               dimethylimidazol-2-                                                            ylamino                                                                    999bu                                                                              4,5-       4 0 H          NHSO.sub.2 NHCH.sub.2 Ph                             dimethylimidazol-2-                                                            ylamino                                                                    999bv                                                                              4,5-       4 0 H          NHSO.sub.2 NHPh                                      dimethylimidazol-2-                                                            ylamino                                                                    999bw                                                                              4,5-       4 0 Ph         H                                                    dimethylimidazol-2-                                                            ylamino                                                                    999bx                                                                              4,5-       4 0 phenylsulfonylamino                                                                       H                                                    dimethylimidazol-2-                                                                           methyl                                                          ylamino                                                                    999by                                                                              4,5-       4 0 3-azabicyclo 3.2.2!                                                                       H                                                    dimethylimidazol-2-                                                                           nonan-3-ylcarbonyl                                              ylamino                                                                    999bz                                                                              4,5-       4 0 adamantan-1-yl                                                                            H                                                    dimethylimidazol-2-                                                                           methylaminocarbonyl                                             ylamino                                                                    999ca                                                                              4,5-       4 0 adamantan-1-yl                                                                            H                                                    dimethylimidazol-2-                                                                           aminocarbonyl                                                   ylamino                                                                    999cb                                                                              4,5-       4 0 adamantan-2-yl                                                                            H                                                    dimethylimidazol-2-                                                                           aminocarbonyl                                                   ylamino                                                                    999cc                                                                              4,5-       4 0 tetrahydroisoquinol                                                                       H                                                    dimethylimidazol-2-                                                                           in-2-ylcarbonyl                                                 ylamino                                                                    999cd                                                                              4,5,6,7-   4 0 H          NHSO.sub.2 Ph                                        tetrahydrobenzimida                                                            zol-2-ylamino                                                              999ce                                                                              4,5,6,7-   4 0 H          NHSO.sub.2 (2,4,6-                                   tetrahydrobenzimida       trimethylphenyl)                                     zol-2-ylamino                                                              999cf                                                                              4,5,6,7-   4 0 H          NHSO.sub.2 (2,4,6-                                   tetrahydrobenzimida       trichlorophenyl)                                     zol-2-ylamino                                                              999cg                                                                              4,5,6,7-   4 0 H          NHSO.sub.2 (2,6-                                     tetrahydrobenzimida       dichlorophenyl)                                      zol-2-ylamino                                                              999ch                                                                              4,5,6,7-   4 0 H          NHSO.sub.2 (2-chloro-6-                              tetrahydrobenzimida       methylphenyl)                                        zol-2-ylamino                                                              999ci                                                                              4,5,6,7-   4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)              tetrahydrobenzimida                                                            zol-2-ylamino                                                              999cj                                                                              4,5,6,7-   4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                    tetrahydrobenzimida                                                            zol-2-ylamino                                                              999ck                                                                              4,5,6,7-   4 0 H          NHSO.sub.2  4-(2,6-                                  tetrahydrobenzimida       dimethylphenyl)phenyl                                zol-2-ylamino                                                              999cl                                                                              4,5,6,7-   4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                    tetrahydrobenzimida                                                            zol-2-ylamino                                                              999cm                                                                              4,5,6,7-   4 0 H          NHSO.sub.2  4-(3,5-                                  tetrahydrobenzimida       dimethyl)isoxazolyl!                                 zol-2-ylamino                                                              999cn                                                                              4,5,6,7-   4 0 H          NHSO.sub.2 (1-napthyl)                               tetrahydrobenzimida                                                            zol-2-ylamino                                                              999co                                                                              4,5,6,7-   4 0 H          NHSO.sub.2 (2-napthyl)                               tetrahydrobenzimida                                                            zol-2-ylamino                                                              999cp                                                                              4,5,6,7-   4 0 H          NHSO.sub.2 NHCH.sub.2 Ph                             tetrahydrobenzimida                                                            zol-2-ylamino                                                              999cq                                                                              4,5,6,7-   4 0 H          NHSO.sub.2 NHPh                                      tetrahydrobenzimida                                                            zol-2-ylamino                                                              999cr                                                                              4,5,6,7-   4 0 Ph         H                                                    tetrahydrobenzimida                                                            zol-2-ylamino                                                              999cs                                                                              4,5,6,7-   4 0 phenylsulfonylamino                                                                       H                                                    tetrahydrobenzimida                                                                           methyl                                                          zol-2-ylamino                                                              999ct                                                                              4,5,6,7-   4 0 3-azabicyclo 3.2.2!                                                                       H                                                    tetrahydrobenzimida                                                                           nonan-3-ylcarbonyl                                              zol-2-ylamino                                                              999cu                                                                              4,5,6,7-   4 0 adamantan-1-yl                                                                            H                                                    tetrahydrobenzimida                                                                           methylaminocarbonyl                                             zol-2-ylamino                                                              999cv                                                                              4,5,6,7-   4 0 adamantan-1-yl                                                                            H                                                    tetrahydrobenzimida                                                                           aminocarbonyl                                                   zol-2-ylamino                                                              999cw                                                                              4,S,6,7-   4 0 adamantan-2-yl                                                                            H                                                    tetrahydrobenzimida                                                                           aminocarbonyl                                                   zol-2-ylamino                                                              999cx                                                                              4,5,6,7-   4 0 tetrahydroisoquinol                                                                       H                                                    tetrahydrobenzimida                                                                           in-2-ylcarbonyl                                                 zol-2-ylamino                                                              999cy                                                                              2-aminopyridin-6-yl                                                                       3 0 H          NHSO.sub.2 (2,4,6-                                                             trimethylphenyl)                                 999cz                                                                              2-aminopyridin-6-yl                                                                       3 0 H          NHSO.sub.2 (2,4,6-                                                             trichlorophenyl)                                 999da                                                                              2-aminopyridin-6-yl                                                                       3 0 H          NHSO.sub.2 (2,6-                                                               dichlorophenyl)                                  999db                                                                              2-aminopyridin-6-yl                                                                       3 0 H          NHSO.sub.2 (2-chloro-6-                                                        methylphenyl)                                    999dc                                                                              2-aminopyridin-6-yl                                                                       3 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)          999de                                                                              2-aminopyridin-6-yl                                                                       3 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                999df                                                                              2-aminopyridin-6-yl                                                                       3 0 H          NHSO.sub.2  4-(2,6-                                                            dimethylphenyl)phenyl                            999dg                                                                              2-aminopyridin-6-yl                                                                       3 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                999dh                                                                              2-aminopyridin-6-yl                                                                       3 0 H          NHSO2 4-(3,5-                                                                  dimethyl)isoxazolyl)                             999di                                                                              2-aminopyridin-6-yl                                                                       3 0 H          NHSO.sub.2 (1-napthyl)                           999dj                                                                              2-aminopyridin-6-yl                                                                       3 0 H          NHSO.sub.2 (2-napthyl)                           999dk                                                                              2-aminopyridin-6-yl                                                                       3 0 H          NHSO.sub.2 NHCH.sub.2 Ph                         999dl                                                                              2-aminopyridin-6-yl                                                                       3 0 H          NHSO.sub.2 NHPh                                  999dm                                                                              2-aminopyridin-6-yl                                                                       3 0 Ph         H                                                999dn                                                                              2-aminopyridin-6-yl                                                                       3 0 phenylsulfonylamino                                                                       H                                                                   methyl                                                      999do                                                                              2-aminopyridin-6-yl                                                                       3 0 3-azabicyclo 3.2.2!                                                                       H                                                                   nonan-3-ylcarbonyl                                          999dp                                                                              2-aminopyridin-6-yl                                                                       3 0 adamantan-1-yl                                                                            H                                                                   methylaminocarbonyl                                         999dq                                                                              2-aminopyridin-6-yl                                                                       3 0 adamantan-1-yl                                                                            H                                                                   aminocarbonyl                                               999dr                                                                              2-aminopyridin-6-yl                                                                       3 0 adamantan-2-yl                                                                            H                                                                   aminocarbonyl                                               999ds                                                                              2-aminopyridin-6-yl                                                                       3 0 tetrahydroisoquinol                                                                       H                                                                   in-2-ylcarbonyl                                             999dt                                                                              imidazol-2-ylamino                                                                        3 0 H          NHSO.sub.2 (2,4,6-                                                             trimethylphenyl)                                 999du                                                                              imidazol-2-ylamino                                                                        3 0 H          NHSO.sub.2 (2,4,6-                                                             trichlorophenyl)                                 999dv                                                                              imidazol-2-ylamino                                                                        3 0 H          NHSO.sub.2 (2,6-                                                               dichlorophenyl)                                  999dw                                                                              imidazol-2-ylamino                                                                        3 0 H          NHSO.sub.2 (2-chloro-6-                                                        methylphenyl)                                    999dx                                                                              imidazol-2-ylamino                                                                        3 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)          999dy                                                                              imidazol-2-ylamino                                                                        3 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                999dz                                                                              imidazol-2-ylamino                                                                        3 0 H          NHSO2 4-(2,6-                                                                  dimethylphenyl)phenyl                            999ea                                                                              imidazol-2-ylamino                                                                        3 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                999eb                                                                              imidazol-2-ylamino                                                                        3 0 H          NHSO.sub.2  4-(3,5-                                                            dimethyl)isoxazolyl)                             999ef                                                                              imidazol-2-ylamino                                                                        3 0 H          NHSO.sub.2 (1-napthyl)                           999eg                                                                              imidazol-2-ylamino                                                                        3 0 H          NHSO.sub.2 (2-napthyl)                           999eh                                                                              imidazol-2-ylamino                                                                        3 0 H          NHSO.sub.2 NHCH.sub.2 Ph                         999ei                                                                              imidazol-2-ylamino                                                                        3 0 H          NHSO.sub.2 NHPh                                  999ej                                                                              imidazol-2-ylamino                                                                        3 0 Ph         H                                                999ek                                                                              imidazol-2-ylamino                                                                        3 0 phenylsulfonylamino                                                                       H                                                                   methyl                                                      999el                                                                              imidazol-2-ylamino                                                                        3 0 3-azabicyclo 3.2.2!                                                                       H                                                                   nonan-3-ylcarbonyl                                          999em                                                                              imidazol-2-ylamino                                                                        3 0 adamantan-1-yl                                                                            H                                                                   methylaminocarbonyl                                         999en                                                                              imidazol-2-ylamino                                                                        3 0 adamantan-1-yl                                                                            H                                                                   aminocarbonyl                                               999eo                                                                              imidazol-2-ylamino                                                                        3 0 adamantan-2-yl                                                                            H                                                                   aminocarbonyl                                               999ep                                                                              imidazol-2-ylamino                                                                        3 0 tetrahydroisoquinol                                                                       H                                                                   in-2-ylcarbonyl                                             999eq                                                                              imidazol-2-ylamino                                                                        2 0 H          NHSO.sub.2 (2,4,6-                                                             trimethylphenyl)                                 999er                                                                              imidazol-2-ylamino                                                                        2 0 H          NHSO.sub.2 (2,4,6-                                                             trichlorophenyl)                                 999es                                                                              imidazol-2-ylamino                                                                        2 0 H          NHSO.sub.2 (2,6-                                                               dichlorophenyl)                                  999et                                                                              imidazol-2-ylamino                                                                        2 0 H          NHSO.sub.2 (2-chloro-6-                                                        methylphenyl)                                    999eu                                                                              imidazol-2-ylamino                                                                        2 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)          999ev                                                                              imidazol-2-ylamino                                                                        2 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                999ew                                                                              imidazol-2-ylamino                                                                        2 0 H          NHSO2 4-(2,6-                                                                  dimethylphenyl)phenyl                            999ex                                                                              imidazol-2-ylamino                                                                        2 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                999ey                                                                              imidazol-2-ylamino                                                                        2 0 H          NHSO.sub.2  4-(3,5-                                                            dimethyl)isoxazolyl!                             999ez                                                                              imidazol-2-ylamino                                                                        2 0 H          NHSO.sub.2 (1-napthyl)                           999fa                                                                              imidazol-2-ylamino                                                                        2 0 H          NHSO.sub.2 (2-napthyl)                           999fb                                                                              imidazol-2-ylamino                                                                        2 0 H          NHSO.sub.2 NHCH.sub.2 Ph                         999fc                                                                              imidazol-2-ylamino                                                                        2 0 H          NHSO.sub.2 NHPh                                  999fd                                                                              imidazol-2-ylamino                                                                        2 0 Ph         H                                                999fe                                                                              imidazol-2-ylamino                                                                        2 0 phenylsulfonylamino                                                                       H                                                                   methyl                                                      999ff                                                                              imidazol-2-ylamino                                                                        2 0 3-azabicyclo 3.2.2!                                                                       H                                                                   nonan-3-ylcarbonyl                                          999fg                                                                              imidazol-2-ylamino                                                                        2 0 adamantan-1-yl                                                                            H                                                                   methylaminocarbonyl                                         999fh                                                                              imidazol-2-ylamino                                                                        2 0 adamantan-1-yl                                                                            H                                                                   aminocarbonyl                                               999fi                                                                              imidazol-2-ylamino                                                                        2 0 adamantan-2-yl                                                                            H                                                                   aminocarbonyl                                               999fj                                                                              imidazol-2-ylamino                                                                        2 0 tetrahydroisoquinol                                                                       H                                                                   in-2-ylcarbonyl                                             999fk                                                                              2-aminoimidazol-4-yl                                                                      2 0 H          NHSO.sub.2 Ph                                    999fl                                                                              2-aminoimidazol-4-yl                                                                      2 0 H          NHSO.sub.2 (2,4,6-                                                             trimethylphenyl)                                 999fm                                                                              2-aminoimidazol-4-yl                                                                      2 0 H          NHSO.sub.2 (2,4,6-                                                             trichlorophenyl)                                 999fn                                                                              2-aminoimidazol-4-yl                                                                      2 0 H          NHSO.sub.2 (2,6-                                                               dichlorophenyl)                                  999fo                                                                              2-aminoimidazol-4-yl                                                                      2 0 H          NHSO.sub.2 (2-chloro-6-                                                        methylphenyl)                                    999fq                                                                              2-aminoimidazol-4-yl                                                                      2 0 H          NHSO.sub.2 C.sub.6 H.sub.6 (2-Br)                999fr                                                                              2-aminoimidazol-4-yl                                                                      2 0 H          NHSO2 4-(2,6-                                                                  dimethylphenyl)phenyl                            999fs                                                                              2-aminoimidazol-4-yl                                                                      2 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                999ft                                                                              2-aminoimidazol-4-yl                                                                      2 0 H          NHSO.sub.2  4-(3,5-                                                            dimethyl)isoxazolyl!                             999fu                                                                              2-aminoimidazol-4-yl                                                                      2 0 H          NHSO.sub.2 (1-napthyl)                           999fv                                                                              2-aminoimidazol-4-yl                                                                      2 0 H          NHSO.sub.2 (2-napthyl)                           999fw                                                                              2-aminoimidazol-4-yl                                                                      2 0 H          NHSO.sub.2 NHCH.sub.2 Ph                         999fx                                                                              2-aminoimidazol-4-yl                                                                      2 0 H          NHSO.sub.2 NHPh                                  999fy                                                                              2-aminoimidazol-4-yl                                                                      2 0 Ph         H                                                999fz                                                                              2-aminoimidazol-4-yl                                                                      2 0 phenylsulfonylamino                                                                       H                                                                   methyl                                                      999ga                                                                              2-aminoimidazol-4-yl                                                                      2 0 3-azabicyclo 3.2.2!                                                                       H                                                                   nonan-3-ylcarbonyl                                          999gb                                                                              2-aminoimidazol-4-yl                                                                      2 0 adamantan-1-yl                                                                            H                                                                   methylaminocarbonyl                                         999gc                                                                              2-aminoimidazol-4-yl                                                                      2 0 adamantan-1-yl                                                                            H                                                                   aminocarbonyl                                               999gd                                                                              2-aminoimidazol-4-yl                                                                      2 0 adamantan-2-yl                                                                            H                                                                   aminocarbonyl                                               999ge                                                                              2-aminoimidazol-4-yl                                                                      2 0 tetrahydroisoquinol                                                                       H                                                                   in-2-ylcarbonyl                                             999gf                                                                              2-aminoimidazol-4-yl                                                                      1 0 H          NHSO.sub.2 Ph                                    999gg                                                                              2-aminoimidazol-4-yl                                                                      1 0 H          NHSO.sub.2 (2,4,6-                                                             trimethylphenyl)                                 999gh                                                                              2-aminoimidazol-4-yl                                                                      1 0 H          NHSO.sub.2 (2,4,6-                                                             trichlorophenyl)                                 999gi                                                                              2-aminoimidazol-4-yl                                                                      1 0 H          NHSO.sub.2 (2,6-                                                               dichlorophenyl)                                  999gj                                                                              2-aminoimidazol-4-yl                                                                      1 0 H          NHSO.sub.2 (2-chloro-6-                                                        methylphenyl)                                    999gk                                                                              2-aminoimidazol-4-yl                                                                      1 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)          999gl                                                                              2-aminoimidazol-4-yl                                                                      1 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                999gm                                                                              2-aminoimidazol-4-yl                                                                      1 0 H          NHSO2 4-(2,6-                                                                  dimethylphenyl)phenyl                            999gn                                                                              2-aminoimidazol-4-yl                                                                      1 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                999go                                                                              2-aminoimidazol-4-yl                                                                      1 0 H          NHSO.sub.2  4-(3,5-                                                            dimethyl)isoxazolyl!                             999gp                                                                              2-aminoimidazol-4-yl                                                                      1 0 H          NHSO.sub.2 (1-napthyl)                           999gq                                                                              2-aminoimidazol-4-yl                                                                      1 0 H          NHSO.sub.2 (2-napthyl)                           999gr                                                                              2-aminoimidazol-4-yl                                                                      1 0 H          NHSO.sub.2 NHCH.sub.2 Ph                         999gs                                                                              2-aminoimidazol-4-yl                                                                      1 0 H          NHSO.sub.2 NHPh                                  999gt                                                                              2-aminoimidazol-4-yl                                                                      1 0 Ph         H                                                999gu                                                                              2-aminoimidazol-4-yl                                                                        0 H          phenylsulfonylamino                                                                        H                                                                  methyl                                           999gv                                                                              2-aminoimidazol-4-yl                                                                        0 H          3-azabicyclo 3.2.2!                                                                        H                                                                  nonan-3-ylcarbonyl                               999gw                                                                              2-aminoimidazol-4-yl                                                                        0 H          adamantan-1-yl                                                                             H                                                                  methylaminocarbonyl                              999gx                                                                              2-aminoimidazol-4-yl                                                                        0 H          adamantan-1-yl                                                                             H                                                                  aminocarbonyl                                    999gy                                                                              2-aminoimidazol-4-yl                                                                        0 H          adamantan-2-yl                                                                             H                                                                  aminocarbonyl                                    999gz                                                                              2-aminoimidazol-4-yl                                                                        0 H          tetrahydroisoquinol                                                                        H                                                                  in-2-ylcarbonyl                                  999ha                                                                              imidazol-2-ylamino-                                                                       3 0 H          NHSO.sub.2 (2,4,6-                                   carbonyl                  trimethylphenyl)                                 999hb                                                                              imidazol-2-ylamino-                                                                       3 0 H          NHSO.sub.2 (2,4,6-                                   carbonyl                  trichlorophenyl)                                 999hc                                                                              imidazol-2-ylamino-                                                                       3 0 H          NHSO.sub.2 (2,6-                                     carbonyl                  dichlorophenyl)                                  999hd                                                                              imidazol-2-ylamino-                                                                       3 0 H          NHSO.sub.2 (2-chloro-6-                              carbonyl                  methylphenyl)                                    999he                                                                              imidazol-2-ylamino-                                                                       3 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)              carbonyl                                                                   999hf                                                                              imidazol-2-ylamino-                                                                       3 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                    carbonyl                                                                   999hf                                                                              imidazol-2-ylamino-                                                                       3 0 H          NHSO2 4-(2,6-                                        carbonyl                  dimethylphenyl)phenyl                            999hh                                                                              imidazol-2-ylamino-                                                                       3 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                    carbonyl                                                                   999hi                                                                              imidazol-2-ylamino-                                                                       3 0 H          NHSO.sub.2  4-(3,5-                                  carbonyl                  dimethyl)isoxazolyl!                             999hj                                                                              imidazol-2-ylamino-                                                                       3 0 H          NHSO.sub.2 (1-napthyl)                               carbonyl                                                                   999hk                                                                              imidazol-2-ylamino-                                                                       3 0 H          NHSO.sub.2 (2-napthyl)                               carbonyl                                                                   999hl                                                                              imidazol-2-ylamino-                                                                       3 0 H          NHSO.sub.2 NHCH.sub.2 Ph                             carbonyl                                                                   999hm                                                                              imidazol-2-ylamino-                                                                       3 0 H          NHSO.sub.2 NHPh                                      carbonyl                                                                   999hn                                                                              imidazol-2-ylamino-                                                                       3 0 Ph         H                                                    carbonyl                                                                   999ho                                                                              imidazol-2-ylamino-                                                                       3 0 phenylsulfonylamino                                                                       H                                                    carbonyl       methyl                                                      999hp                                                                              imidazol-2-ylamino-                                                                       3 0 3-azabicyclo 3.2.2!                                                                       H                                                    carbonyl       nonan-3-ylcarbonyl                                          999hq                                                                              imidazol-2-ylamino-                                                                       3 0 adamantan-1-yl                                                                            H                                                    carbonyl       methylaminocarbonyl                                         999hr                                                                              imidazol-2-ylamino-                                                                       3 0 adamantan-1-yl                                                                            H                                                    carbonyl       aminocarbonyl                                               999hs                                                                              imidazol-2-ylamino-                                                                       3 0 adamantan-2-yl                                                                            H                                                    carbonyl       aminocarbonyl                                               999ht                                                                              imidazol-2-ylamino-                                                                       3 0 tetrahydroisoquinol                                                                       H                                                    carbonyl       in-2-ylcarbonyl                                             99hu                                                                               benzimidazol-2-                                                                           0 0 H          NHSO.sub.2 Ph                                        ylmethylaminocarbonyl                                                      999hv                                                                              benzimidazol-2-                                                                           0 0 H          NHSO.sub.2 (2,4,6-                                   ylmethylaminocarbonyl     trimethylphenyl)                                 999hw                                                                              benzimidazol-2-                                                                           0 0 H          NHSO.sub.2 (2,4,6-                                   ylmethylaminocarbonyl     trichlorophenyl)                                 999hx                                                                              benzimidazol-2-                                                                           0 0 H          NHSO.sub.2 (2,6-                                     ylmethylaminocarbonyl     dichlorophenyl)                                  999hy                                                                              benzimidazol-2-                                                                           0 0 H          NHSO.sub.2 (2-chloro-6-                              ylmethylaminocarbonyl     methylphenyl)                                    999hz                                                                              benzimidazol-2-                                                                           0 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)              ylmethylaminocarbonyl                                                      999ia                                                                              benzimidazol-2-                                                                           0 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                    ylmethylaminocarbonyl                                                      999ib                                                                              benzimidazol-2-                                                                           0 0 H          NHSO2 4-(2,6-                                        ylmethylaminocarbonyl     dimethylphenyl)phenyl                            999ic                                                                              benzimidazol-2-                                                                           0 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                    ylmethylaminocarbonyl                                                      999id                                                                              benzimidazol-2-                                                                           0 0 H          NHSO.sub.2  4-(3,5-                                  ylmethylaminocarbonyl     dimethyl)isoxazoyl!                              999ie                                                                              benzimidazol-2-                                                                           0 0 H          NHSO.sub.2 (1-napthyl)                               ylmethylaminocarbonyl                                                      999if                                                                              benzimidazol-2-                                                                           0 0 H          NHSO.sub.2 (2-napthyl)                               ylmethylaminocarbonyl                                                      999ig                                                                              benzimidazol-2-                                                                           0 0 H          NHSO.sub.2 NHCH.sub.2 Ph                             ylmethylaminocarbonyl                                                      999ih                                                                              benzimidazol-2-                                                                           0 0 H          NHSO.sub.2 NHPh                                      ylmethylaminocarbonyl                                                      999ii                                                                              benzimidazol-2-                                                                           0 0 Ph         H                                                    ylmethylaminocarbonyl                                                      999ij                                                                              benzimidazol-2-                                                                           0 0 phenylsulfonylamino                                                                       H                                                    ylmethylaminocarbonyl                                                                         methyl                                                      999ik                                                                              benzimidazol-2-                                                                           0 0 3-azabicyclo 3.2.2!                                                                       H                                                    methylaminocarbonyl                                                                           nonan-3-ylcarbonyl                                          999il                                                                              benzimidazol-2-                                                                           0 0 adamantan-1-yl                                                                            H                                                    ylmethylaminocarbonyl                                                                         methylaminocarbonyl                                         999im                                                                              benzimidazol-2-                                                                           0 0 adamantan-1-yl                                                                            H                                                    ylmethylaminocarbonyl                                                                         aminocarbonyl                                               999in                                                                              benzimidazol-2-                                                                           0 0 adamantan-2-yl                                                                            H                                                    ylmethylaminocarbonyl                                                                         aminocarbonyl                                               999io                                                                              benzimidazol-2-                                                                           0 0 tetrahydroisoquinol                                                                       H                                                    ylmethylaminocarbonyl                                                                         in-2-ylcarbonyl                                             999ip                                                                              N-(benzimidazol-2-                                                                        0 0 H          NHSO.sub.2 Ph                                        ylmethyl)-N-methyl-                                                            aminocarbonyl                                                              999iq                                                                              N-benzimidazol-2-                                                                         0 0 H          NHSO.sub.2 (2,4,6-                                   ymethyl-N-methyl-         trimethylphenyl)                                     aminocarbonyl                                                              999ir                                                                              N-benzimidazol-2-                                                                         0 0 H          NHSO.sub.2 (2,4,6-                                   ymethyl-N-methyl-         trichlorophenyl)                                     aminocarbonyl                                                              999is                                                                              N-benzimidazol-2-                                                                         0 0 H          NHSO.sub.2 (2,6-                                     ylmethyl-N-methyl-        dichlorophenyl)                                      aminocarbonyl                                                              999it                                                                              N-benzimidazol-2-                                                                         0 0 H          NHSO.sub.2 (2-chloro-6-                              ylmethyl-N-methyl-        methylphenyl)                                        aminocarbonyl                                                              999iu                                                                              N-benzimidazol-2-                                                                         0 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)              ylmethyl-N-methyl-                                                             aminocarbonyl                                                              999iv                                                                              N-benzimidazol-2-                                                                         0 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                    ylmethyl)-N-methyl-                                                            aminocarbonyl                                                              999iw                                                                              N-benzimidazol-2-                                                                         0 0 H          NHSO2 4-(2,6-                                        ylmethyl)-N-methyl-       dimethylphenyl)phenyl                                aminocarbonyl                                                              999ix                                                                              N-benzimidazol-2-                                                                         0 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                    ylmethyl)-N-methyl-                                                            aminocarbonyl                                                              999iy                                                                              N-benzimidazol-2-                                                                         0 0 H          NHSO.sub.2  4-(3,5-                                  ylmethyl-N-methyl-        dimethyl)isoxazolyl!                                 aminocarbonyl                                                              999iz                                                                              N-benzimidazol-2-                                                                         0 0 H          NHSO.sub.2 (1-napthyl)                               ylmethyl)-N-methyl-                                                            aminocarbonyl                                                              999ja                                                                              N-benzimidazol-2-                                                                         0 0 H          NHSO.sub.2 (2-napthyl)                               ylmethyl)-N-methyl-                                                            aminocarbonyl                                                              999jb                                                                              N-benzimidazol-2-                                                                         0 0 H          NHSO.sub.2 NHCH.sub.2 Ph                             ylmethyl)-N-methyl-                                                            aminocarbonyl                                                              999jc                                                                              N-benzimidazol-2-                                                                         0 0 H          NHSO.sub.2 NHPh                                      ylmethyl)-N-methyl-                                                            aminocarbonyl                                                              999jd                                                                              N-benzimidazol-2-                                                                         0 0 Ph         H                                                    ylmethyl)-N-methyl-                                                            aminocarbonyl                                                              999je                                                                              N-benzimidazol-2-                                                                         0 0 phenylsulfonylamino                                                                       H                                                    ylmethyl)-N-methyl-                                                                           methyl                                                          aminocarbonyl                                                              999jf                                                                              N-benzimidazol-2-                                                                         0 0 3-azabicyclo 3.2.2!                                                                       H                                                    ylmethyl)-N-methyl-                                                                           nonan-3-ylcarbonyl                                              aminocarbonyl                                                              999jg                                                                              N-benzimidazol-2-                                                                         0 0 adamantan-1-yl                                                                            H                                                    ylmethyl)-N-methyl-                                                                           methylaminocarbonyl                                             aminocarbonyl                                                              999jh                                                                              N-benzimidazol-2-                                                                         0 0 adamantan-1-yl                                                                            H                                                    ylmethyl)-N-methyl-                                                                           aminocarbonyl                                                   aminocarbonyl                                                              999ji                                                                              N-benzimidazol-2-                                                                         0 0 adamantan-2-yl                                                                            H                                                    ylmethyl)-N-methyl-                                                                           aminocarbonyl                                                   aminocarbonyl                                                              999jj                                                                              N-benzimidazol-2-                                                                         0 0 tetrahydroisoquinol                                                                       H                                                    ylmethyl)-N-methyl-                                                                           in-2-ylcarbonyl                                                 aminocarbonyl                                                              999jk                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 H          NHSO.sub.2 Ph                                                                              494.3                                    pyridin-2-ylamino                                                          999jl                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 H          NHSO.sub.2 (2,4,6-                                                                         536.5                                    pyridin-2-ylamino         trimethylphenyl)                                 999jm                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 H          NHSO.sub.2 (2,4,6-                                   pyridin-2-ylamino         trichlorophenyl)                                 999jn                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 H          NHSO.sub.2 (2,6-                                     pyridin-2-ylamino         dichlorophenyl)                                  999jo                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 H          NHSO.sub.2 (2-chloro-6-                              pyridin-2-ylamino         methylphenyl)                                    999jp                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)              pyridin-2-ylamino                                                          999jq                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                    pyridin-2-ylamino                                                          999jr                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 H          NHSO2 4-(2,6-                                        pyridin-2-ylamino         dimethylphenyl)phenyl                            999js                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 H          NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                    pyridin-2-ylamino                                                          999jt                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 H          NHSO.sub.2  4-(3,5-                                  pyridin-2-ylamino         dimethyl)isoxazolyl!                             999ju                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 H          NHSO.sub.2 (1-napthyl)                               pyridin-2-ylamino                                                          999jv                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 H          NHSO.sub.2 (2-napthyl)                               pyridin-2-ylamino                                                          999jw                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 H          NHSO.sub.2 NHCH.sub.2 Ph                             pyridin-2-ylamino                                                          999jx                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 H          NHSO.sub.2 NHPh                                      pyridin-2-ylamino                                                          999jy                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 Ph         N                                                    pyridin-2-ylamino                                                          999jz                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 phenylsulfonylamino                                                                       H                                                    pyridin-2-ylamino                                                                             methyl                                                      999ka                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 3-azabicyclo 3.2.2!                                                                       H                                                    pyridin-2-ylamino                                                                             nonan-3-ylcarbonyl                                          999kb                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 adamantan-1-yl                                                                            H                                                    pyridin-2-ylamino                                                                             methylaminocarbonyl                                         999kc                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 adamantan-1-yl                                                                            H                                                    pyridin-2-ylamino                                                                             aminocarbonyl                                               999kd                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 adamantan-2-yl                                                                            H                                                    pyridin-2-ylamino                                                                             aminocarbonyl                                               999ke                                                                              3,4,5,6,-tetrahydro-                                                                      4 0 tetrahydroisoquinol                                                                       H                                                    pyridin-2-ylamino                                                                             in-2-ylcarbonyl                                             __________________________________________________________________________

                                      TABLE 3                                      __________________________________________________________________________      ##STR36##                                                                     Ex. No.                                                                            R.sup.1 -U m n Q  R.sup.8   R.sup.9   R.sup.14                                                                          MS                                __________________________________________________________________________     1001                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         H         H  326.2                             1002                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         H         H                                    1003                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHCbz     H                                    1004                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHCbz     H  475.2                             1005                                                                               imidazolin-2-ylamino                                                                      2 0 S  H         NHCbz     H                                    1006                                                                               imidazolin-2-ylamino                                                                      3 0 S  H         NHCbz     H                                    1007                                                                               imidazolin-2-ylamino                                                                      2 0 NH H         NHCbz     H                                    1008                                                                               imidazolin-2-ylamino                                                                      3 0 NH H         NHCbz     H                                    1009                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         H         H                                        2-ylamino                                                                  1010                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHCbz     H                                        2-ylamino                                                                  1011                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         H         H                                        2-ylamino                                                                  1012                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHCbz     H                                        2-ylamino                                                                  1013                                                                               tetrahydropyrimidin-                                                                      2 0 S  H         NHCbz     H                                        2-ylamino                                                                  1014                                                                               tetrahydropyrimidin-                                                                      3 0 S  H         NHCbz     H                                        2-ylamino                                                                  1015                                                                               tetrahydropyrimidin-                                                                      2 0 NH H         NHCbz     H                                        2-ylamino                                                                  1016                                                                               tetrahydropyrimidin-                                                                      3 0 NH H         NHCbz     H                                        2-ylamino                                                                  1017                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHCO2-n-Bu                                                                               H                                    1018                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHCO2-n-Bu                                                                               H                                    1019                                                                               imidazolin-2-ylamino                                                                      2 0 S  H         NHCO2-n-Bu                                                                               H                                    1020                                                                               imidazolin-2-ylamino                                                                      3 0 S  H         NHCO2-n-Bu                                                                               H                                    1021                                                                               imidazolin-2-ylamino                                                                      2 0 NH H         NHCO2-n-Bu                                                                               H                                    1022                                                                               imidazolin-2-ylamino                                                                      3 0 NH H         NHCO2-n-Bu                                                                               H                                    1023                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHCO2-n-Bu                                                                               H                                        2-ylamino                                                                  1024                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHCO2-n-Bu                                                                               H                                        2-ylamino                                                                  1025                                                                               tetrahydropyrimidin-                                                                      2 0 S  H         NHCO2-n-Bu                                                                               H                                        2-ylamino                                                                  1026                                                                               tetrahydropyrimidin-                                                                      3 0 S  H         NHCO2-n-Bu                                                                               H                                        2-ylamino                                                                  1027                                                                               tetrahydropyrimidin-                                                                      2 0 NH H         NHCO2-n-Bu                                                                               H                                        2-ylamino                                                                  1028                                                                               tetrahydropyrimidin-                                                                      3 0 NH H         NHCO2-n-Bu                                                                               H                                        2-ylamino                                                                  1029                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 Ph(o-CH.sub.3)                                                                H                                    1030                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 Ph(o-CH.sub.3)                                                                H                                    1031                                                                               imidazolin-2-ylamino                                                                      2 0 S  H         NHSO.sub.2 Ph(o-CH.sub.3)                                                                H                                    1032                                                                               imidazolin-2-ylamino                                                                      3 0 S  H         NHSO.sub.2 Ph(o-CH.sub.3)                                                                H                                    1033                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 Ph(m-CH.sub.3)                                                                H                                    1034                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 Ph(m-CH.sub.3)                                                                H  495.3                             1035                                                                               imidazolin-2-ylamino                                                                      2 0 S  H         NHSO.sub.2 Ph(m-CH.sub.3)                                                                H                                    1036                                                                               imidazolin-2-ylamino                                                                      3 0 S  H         NHSO.sub.2 Ph(m-CH.sub.3)                                                                H                                    1037                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 Ph(p-CH.sub.3)                                                                H                                    1038                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 Ph(p-CH.sub.3)                                                                H                                    1039                                                                               imidazolin-2-ylamino                                                                      2 0 S  H         NHSO.sub.2 Ph(p-CH.sub.3)                                                                H                                    1040                                                                               imidazolin-2-ylamino                                                                      3 0 S  H         NHSO.sub.2 Ph(p-CH.sub.3)                                                                H                                    1041                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 Ph(o-Cl)                                                                      H                                    1042                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 Ph(o-Cl)                                                                      H                                    1043                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 Ph(m-Cl)                                                                      H                                    1044                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 Ph(m-Cl)                                                                      H                                    1045                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 Ph(p-Cl)                                                                      H                                    1046                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 Ph(p-Cl)                                                                      H                                    1047                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 Ph(p-Cl)                                                                      H                                        2-ylamino                                                                  1048                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHSO.sub.2 Ph(p-Cl)                                                                      H                                        2-ylamino                                                                  1049                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 Ph(m-Cl)                                                                      H                                        2-ylamino                                                                  1050                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHSO.sub.2 Ph(m-Cl)                                                                      H                                        2-ylamino                                                                  1051                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 Ph(p-Cl)                                2-ylamino                                                                  1052                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHSO.sub.2 Ph(p-Cl)                                                                      H                                        2-ylamino                                                                  1053                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 Ph(m-F)                                                                       H                                    1054                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 Ph(m-F)                                                                       H                                    1055                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 Ph(m-F)                                                                       H                                        2-ylamino                                                                  1056                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHSO.sub.2 Ph(m-F)                                                                       H                                        2-ylamino                                                                  1057                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 Ph(p-F)                                                                       H                                    1058                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 Ph(p-F)                                                                       H                                    1059                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 Ph(p-F)                                                                       H                                        2-ylamino                                                                  1060                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHSO.sub.2 Ph(p-F)                                                                       H                                        2-ylamino                                                                  1061                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 Ph(m-Br)                                                                      H                                    1062                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 Ph(m-Br)                                                                      H                                    1063                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 Ph(m-Br)                                                                      H                                        2-ylamino                                                                  1064                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHSO.sub.2 Ph(m-Br)                                                                      H                                        2-ylamino                                                                  1065                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 Ph(p-Br)                                                                      H                                    1066                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 Ph(p-Br)                                                                      H                                    1067                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 Ph(p-Br)                                                                      H                                        2-ylamino                                                                  1068                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHSO.sub.2 Ph(p-Br)                                                                      H                                        2-ylamino                                                                  1069                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 Ph(m-OCH.sub.3)                                                               H                                    1070                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 Ph(m-OCH.sub.3)                                                               H                                    1071                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 Ph(m-OCH.sub.3)                                                               H                                        2-ylamino                                                                  1072                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHSO.sub.2 Ph(m-OCH.sub.3)                                                               H                                        2-ylamino                                                                  1073                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 Ph(p-OCH.sub.3)                                                               H                                    1074                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 Ph(p-OCH.sub.3)                                                               H                                    1075                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 Ph(p-OCH.sub.3)                                                               H                                        2-ylamino                                                                  1076                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHSO.sub.2 Ph(p-OCH.sub.3)                                                               H                                        2-ylamino                                                                  1077                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 Bn                                                                            H                                    1078                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 Bn                                                                            H                                    1079                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 Bn                                                                            H                                        2-ylamino                                                                  1080                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHSO.sub.2 Bn                                                                            H                                        2-ylamino                                                                  1081                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 Et                                                                            H                                    1082                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 Et                                                                            H                                    1083                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 Et                                                                            H                                        2-ylamino                                                                  1084                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHSO.sub.2 Et                                                                            H                                        2-ylamino                                                                  1085                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 -n-Pr                                                                         H                                    1086                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 -n-Pr                                                                         H                                    1087                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 -n-Pr                                                                         H                                        2-ylamino                                                                  1088                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHSO.sub.2 -n-Pr                                                                         H                                        2-ylamino                                                                  1089                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 -n-(C.sub.5 H.sub.11)                                                         H                                    1090                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 -n-(C.sub.5 H.sub.11)                                                         H                                    1091                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 -n-(C.sub.5 H.sub.11)                                                         H                                        2-ylamino                                                                  1092                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHSO.sub.2 -n-(C.sub.5 H.sub.11)                                                         H                                        2-ylamino                                                                  1093                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHCO.sub.2 Et                                                                            H                                    1094                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHCO.sub.2 Et                                                                            H                                    1095                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHCO.sub.2 Et                                                                            H                                        2-ylamino                                                                  1096                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHCO.sub.2 Et                                                                            H                                        2-ylamino                                                                  1097                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHCO.sub.2 -n-C.sub.5 H.sub.11                                                           H                                    1098                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHCO.sub.2 -n-C.sub.5 H.sub.11                                                           H                                    1099                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHCO.sub.2 -n-C.sub.5 H.sub.11                                                           H                                        2-ylamino                                                                  1100                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHCO.sub.2 -n-C.sub.5 H.sub.11                                                           H                                        2-ylamino                                                                  1101                                                                               imidazolin-2-ylamino                                                                      4 0 O  H         NHCbz     H                                    1102                                                                               tetrahydropyrimidin-                                                                      4 0 O  H         NHCbz     H                                        2-ylamino                                                                  1103                                                                               imidazolin-2-ylamino                                                                      4 0 O  H         NHCO.sub.2 -n-Bu                                                                         H                                    1104                                                                               tetrahydropyrimidin-                                                                      4 0 O  H         NHCO.sub.2 -n-Bu                                                                         H                                        2-ylamino                                                                  1105                                                                               imidazolin-2-ylamino                                                                      4 0 O  H         NHSO.sub.2 Ph                                                                            H                                    1106                                                                               tetrahydropyrimidin-                                                                      4 0 O  H         NHSO.sub.2 Ph                                                                            H                                        2-ylamino                                                                  1107                                                                               imidazolin-2-ylamino                                                                      4 0 O  H         NHSO.sub.2 -n-Bu                                                                         H                                    1108                                                                               tetrahydropyrimidin-                                                                      4 0 O  H         NHSO.sub.2 -n-Bu                                                                         H                                        2-ylamino                                                                  1109                                                                               imidazolin-2-ylamino                                                                      4 0 S  H         NHCbz     H                                    1110                                                                               tetrahydropyrimidin-                                                                      4 0 S  H         NHCbz     H                                        2-ylamino                                                                  1111                                                                               imidazolin-2-ylamino                                                                      4 0 S  H         NHSO.sub.2 Bu                                                                            H                                    1112                                                                               tetrahydropyrimidin-                                                                      4 0 S  H         NHSO.sub.2 Bu                                                                            H                                        2-ylamino                                                                  1113                                                                               imidazolin-2-ylamino                                                                      2 0 O  Me        H         H                                    1114                                                                               imidazolin-2-ylamino                                                                      3 0 O  Me        H         H                                    1115                                                                               tetrahydropyrimidin-                                                                      2 0 O  Me        H         H                                        2-ylamino                                                                  1116                                                                               tetrahydropyrimidin-                                                                      3 0 O  Me        H         H                                        2-ylamino                                                                  1117                                                                               imidazolin-2-ylamino                                                                      3 0 S  Me        H                                              1118                                                                               tetrahydropyrimidin-                                                                      3 0 S  Me        H         H                                        2-ylamino                                                                  1119                                                                               imidazolin-2-ylamino                                                                      2 0 O  Me        NHCbz     H                                    1120                                                                               imidazolin-2-ylamino                                                                      3 0 O  Me        NHCbz     H                                    1121                                                                               tetrahydropyrimidin-                                                                      2 0 O  Me        NHSO.sub.2 -n-Bu                                                                         H                                        2-ylamino                                                                  1122                                                                               tetrahydropyrimidin-                                                                      3 0 O  Me        NHSO.sub.2 -n-Bu                                                                         H                                        2-ylamino                                                                  1123                                                                               imidazolin-2-ylamino                                                                      2 0 O  Et        H         H                                    1124                                                                               imidazolin-2-ylamino                                                                      3 0 O  Et        H         H                                    1125                                                                               tetrahydropyrimidin-                                                                      2 0 O  Et        H         H                                        2-ylamino                                                                  1126                                                                               tetrahydropyrimidin-                                                                      3 0 O  Et        H         H                                        2-ylamino                                                                  1127                                                                               imidazolin-2-ylamino                                                                      3 0 S  Et        H         H                                    1128                                                                               tetrahydropyrimidin-                                                                      3 0 S  Et        H         H                                        2-ylamino                                                                  1129                                                                               imidazolin-2-ylamino                                                                      2 0 O  Ph        H         H                                    1130                                                                               imidazolin-2-ylamino                                                                      3 0 O  Ph        H         H                                    1131                                                                               tetrahydropyrimidin-                                                                      2 0 0  Ph        H         H                                        2-ylamino                                                                  1132                                                                               tetrahydropyrimidin-                                                                      3 0 O  Ph        H         H                                        2-ylamino                                                                  1133                                                                               imidazolin-2-ylamino                                                                      3 0 S  Ph        H         H                                    1134                                                                               tetrahydropyrimidin-                                                                      3 0 S  Ph        H         H                                        2-ylamino                                                                  1135                                                                               imidazolin-2-ylamino                                                                      2 0 O  Bn        H         H                                    1136                                                                               imidazolin-2-ylamino                                                                      3 0 O  Bn        H         H                                    1137                                                                               tetrahydropyrimidin-                                                                      2 0 O  Bn        H         H                                        2-ylamino                                                                  1138                                                                               tetrahydropyrimidin-                                                                      3 0 O  Bn        H         H                                        2-ylamino                                                                  1139                                                                               imidazolin-2-ylamino                                                                      3 0 S  Bn        H         H                                    1140                                                                               tetrahydropyrimidin-                                                                      3 0 S  Bn        H         H                                        2-ylamino                                                                  1141                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHCbz     Me                                   1142                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHCbz     Me                                   1143                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHCbz     Me                                       2-ylamino                                                                  1144                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHCbz     Me                                       2-ylamino                                                                  1145                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 -n-Bu                                                                         Me                                   1146                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 -n-Bu                                                                         Me                                   1147                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 -n-Bu                                                                         Me                                       2-ylamino                                                                  1148                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHSO.sub.2 -n-Bu                                                                         Me                                       2-ylamino                                                                  1149                                                                               imidazolin-2-ylamino                                                                      3 0 S  H         NHCbz     Me                                   1150                                                                               tetrahydropyrimidin-                                                                      3 0 S  H         NHCbz     Me                                       2-ylamino                                                                  1151                                                                               imidazolin-2-ylamino                                                                      3 0 S  H         NHSO.sub.2 -n-Bu                                                                         Me                                   1152                                                                               tetrahydropyrimidin-                                                                      3 0 S  H         NHSO.sub.2 -n-Bu                                                                         Me                                       2-ylamino                                                                  1153                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHCbz.    Bn                                   1154                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHCbz     Bn                                   1155                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHCbz     Bn                                       2-ylamino                                                                  1156                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHCbz     Bn                                       2-ylamino                                                                  1157                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 -n-Bu                                                                         Bn                                   1158                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 -n-Bu                                                                         Bn                                   1159                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 -n-Bu                                                                         Bn                                       2-ylamino                                                                  1160                                                                               tetrahydropyrimidin-                                                                      3 0 O  H         NHSO.sub.2 -n-Bu                                                                         Bn                                       2-ylamino                                                                  1161                                                                               imidazolin-2-ylamino                                                                      3 0 S  H         NHCbz     Bn                                   1162                                                                               tetrahydropyrimidin-                                                                      3 0 S  H         NHCbz     Bn                                       2-ylamino                                                                  1163                                                                               imidazolin-2-ylamino                                                                      3 0 S  H         NHSO.sub.2 -n-Bu                                                                         Bn                                   1164                                                                               tetrahydropyrimidin-                                                                      3 0 S  H         NHSO.sub.2 -n-Bu                                                                         Bn                                       2-ylamino                                                                  1165                                                                               imidazolin-2-ylamino                                                                      3 0 O  Me        NHCbz     Me                                   1166                                                                               tetrahydropyrimidin-                                                                      3 0 O  Me        NHSO.sub.2 Bu                                                                            Me                                       2-ylamino                                                                  1167                                                                               imidazolin-2-ylamino                                                                      3 0 O  Bn        NHCbz     Me                                   1168                                                                               tetrahydropyrimidin-                                                                      3 0 O  Bn        NHCbz     Me                                       2-ylamino                                                                  1169                                                                               imidazolin-2-ylamino                                                                      3 0 O  Me        NHSO.sub.2 -n-Bu                                                                         Me                                   1170                                                                               tetrahydropyrimidin-                                                                      3 0 O  Me        NHCbz     Me                                       2-ylamino                                                                  1171                                                                               imidazolin-2-ylamino                                                                      3 0 O  Bn        NHSO.sub.2 -n-Bu                                                                         Me                                   1172                                                                               tetrahydropyrimidin-                                                                      3 0 O  Bn        NHCbz     Me                                       2-ylamino                                                                  1173                                                                               (4-oxoimidazolin-2-                                                                       2 0 O  H         NHCBz     H                                        yl)amino                                                                   1174                                                                               (4-oxoimidazolin-2-                                                                       3 0 O  H         NHCBz     H                                        yl)amino                                                                   1175                                                                               (4-oxoimidazolin-2-                                                                       2 0 O  H         NHCO.sub.2 -n-Bu                                                                         H                                        yl)amino                                                                   1176                                                                               (4-oxoimidazolin-2-                                                                       3 0 O  H         NHCO.sub.2 -n-Bu                                                                         H                                        yl)amino                                                                   1177                                                                               (4-oxoimidazolin-2-                                                                       2 0 O  H         NHSO.sub.2 Ph                                                                            H                                        yl)amino                                                                   1178                                                                               (4-oxoimidazolin-2-                                                                       3 0 O  H         NHSO.sub.2 Ph                                                                            H                                        yl)amino                                                                   1179                                                                               (4-oxoimidazolin-2-                                                                       2 0 O  H         NHSO.sub.2 -n-Bu                                                                         H                                        yl)amino                                                                   1180                                                                               (4-oxoimidazolin-2-                                                                       3 0 O  H         NHSO.sub.2 -n-Bu                                                                         H                                        yl)amino                                                                   1181                                                                               (4-        3 0 O  H         NHCbz     H                                        oxotetrahydropyrimidin-                                                        2-yl)amino                                                                 1182                                                                               (4-        3 0 O  H         NHCO.sub.2 -n-Bu                                                                         H                                        oxotetrahydropyrimidin-                                                        2-yl)amino                                                                 1183                                                                               (4-        3 0 O  H         NHSO.sub.2 Ph                                                                            H                                        oxotetrahydropyrimidin-                                                        2-yl)amino                                                                 1184                                                                               (4-        3 0 O  H         NHSO.sub.2 -n-Bu                                                                         H                                        oxotetrahydropyrimidin-                                                        2-yl)amino                                                                 1185                                                                               (4-oxoimidazolin-2-                                                                       3 0 S  H         NHCbz     H                                        yl)amino                                                                   1186                                                                               (4-oxoimidazolin-2-                                                                       3 0 S  H         NHSO.sub.2 -n-Bu                                                                         H                                        yl)amino                                                                   1187                                                                               (4-        3 0 S  H         NHCbz     H                                        oxotetrahydropyrimidin-                                                        2-yl)amino                                                                 1188                                                                               (4-        3 0 S  H         NHSO.sub.2 -n-Bu                                                                         H                                        oxotetrahydropyrimidin-                                                        2-yl)amino                                                                 1189                                                                               (4-oxoimidazolin-2-                                                                       3 0 O  Me        H         H                                        yl)amino                                                                   1190                                                                               (4-        3 0 O  Me        H         H                                        oxotetrahydropyrimidin-                                                        2-yl)amino                                                                 1191                                                                               (4-oxoimidazolin-2-                                                                       3 0 O  Bn        H         H                                        yl)amino                                                                   1192                                                                               (4-        3 0 O  Bn        H                                                  oxotetrahydropyrimidin-                                                        2-yl)amino                                                                 1193                                                                               (4-oxomidazolin-2-                                                                        3 0 O  Me        NHCbz     H                                        yl)amino                                                                   1194                                                                               (4-        3 0 O  Me        NHSO.sub.2 -n-Bu                                                                         H                                        oxotetrahydropyrimidin-                                                        2-yl)amino                                                                 1195                                                                               (4-oxoimidazolin-2-                                                                       3 0 O  H         NHCbz     Me                                       yl)amino                                                                   1196                                                                               (4-        3 0 O  H         NHCbz     Bn                                       oxotetrahydropyrimidin-                                                        2-yl)amino                                                                 1197                                                                               imidazolin-2-                                                                             1 0 O  H         NHCbz     H                                        ylaminocarbonyl                                                            1198                                                                               imidazolin-2-                                                                             2 0 O  H         NHCbz     H                                        ylaminocarbonyl                                                            1199                                                                               tetrahydropyrimidin-                                                                      1 0 O  H         NHSO.sub.2 -n-Bu                                                                         H                                        2-ylaminocarbonyl                                                          1200                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 -n-Bu                                                                         H                                        2-ylaminocarbonyl                                                          1201                                                                               imidazolin-2-                                                                             2 0 O  H         NHCbz     H                                        ylaminocarbonyl                                                            1202                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 -n-Bu                                                                         H                                        2-ylaminocarbonyl                                                          1203                                                                               imidazolin-2-                                                                             1 0 O  H         NHCO.sub.2 -n-Bu                                                                         H                                        ylaminocarbonyl                                                            1204                                                                               imidazolin-2-                                                                             2 0 O  H         NHCO.sub.2 -n-Bu                                                                         H                                        ylaminocarbonyl                                                            1205                                                                               tetrahydropyrimidin-                                                                      1 0 O  H         NHSO.sub.2 Ph                                                                            H                                        2-ylaminocarbonyl                                                          1206                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 Ph                                                                            H                                        2-ylaminocarbonyl                                                          1207                                                                               imidazolin-2-                                                                             2 0 O  Me        NHCbz     H                                        ylaminocarbonyl                                                            1208                                                                               tetrahydropyrimidin-                                                                      2 0 O  Me        NHSO.sub.2 -n-Bu                                                                         H                                        2-ylaminocarbonyl                                                          1209                                                                               imidazolin-2-                                                                             2 0 O  Bn        H         H                                        ylaminocarbonyl                                                            1210                                                                               tetrahydropyrimidin-                                                                      2 0 O  Bn        H         H                                        2-ylaminocarbonyl                                                          1211                                                                               imidazolin-2-                                                                             2 0 O  Me        H         H                                        ylaminocarbonyl                                                            1212                                                                               tetrahydropyrimidin-                                                                      2 0 O  Me        H         H                                        2-ylaminocarbonyl                                                          1213                                                                               imidazolin-2-                                                                             2 0 O  H         NHCbz     Me                                       ylaminocarbonyl                                                            1214                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHCbz     Me                                       2-ylaminocarbonyl                                                          1215                                                                               imidazolin-2-                                                                             2 0 O  H         NHSO.sub.2 -n-Bu                                                                         Me                                       ylaminocarbonyl                                                            1216                                                                               tetrahydropyrimidin-                                                                      2 0 O  H         NHSO.sub.2 -n-Bu                                                                         Me                                       2-ylaminocarbonyl                                                          1217                                                                               imidazolin-2-                                                                             2 0 S  Me        H         H                                        ylaminocarbonyl                                                            1218                                                                               tetrahydropyrimidin-                                                                      2 0 S  Bn        H         H                                        2-ylaminocarbonyl                                                          1219                                                                               imidazolin-2-                                                                             2 0 S  H         NHCbz     Me                                       ylaminocarbonyl                                                            1220                                                                               tetrahydropyrimidin-                                                                      2 0 S  H         NHSO.sub.2 -n-Bu                                                                         Me                                       2-ylaminocarbonyl                                                          1221                                                                               imidazolin-2-ylamino                                                                      2 1 O  H         NHCbz     H                                    1222                                                                               imidazolin-2-ylamino                                                                      3 1 O  H         NHCbz     H                                    1223                                                                               tetrahydropyrimidin-                                                                      2 1 O  H         NHCbz     H                                        2-ylamino                                                                  1224                                                                               tetrahydropyrimidin-                                                                      3 1 O  H         NHCbz     H                                        2-ylamino                                                                  1225                                                                               imidazolin-2-ylamino                                                                      2 1 O  H         NHSO.sub.2 -n-Bu                                                                         H                                    1226                                                                               imidazolin-2-ylamino                                                                      3 1 O  H         NHSO.sub.2 -n-Bu                                                                         H                                    1227                                                                               tetrahydropyrimidin-                                                                      2 1 O  H         NHSO.sub.2 -n-Bu                                                                         H                                        2-ylamino                                                                  1228                                                                               tetrahydropyrimidin-                                                                      3 1 O  H         NHSO.sub.2 -n-Bu                                                                         H                                        2-ylamino                                                                  1229                                                                               imidazolin-2-ylamino                                                                      2 1 S  H         NHCbz     H                                    1230                                                                               imidazolin-2-ylamino                                                                      3 1 S  H         NHCbz     H                                    1231                                                                               tetrahydropyrimidin-                                                                      2 1 S  H         NHCbz     H                                        2-ylamino                                                                  1232                                                                               tetranydropyrimidin-                                                                      3 1 S  H         NHCbz     H                                        2-ylamino                                                                  1233                                                                               imidazolin-2-ylamino                                                                      2 1 O  Me        H         H                                    1234                                                                               imidazolin-2-ylamino                                                                      3 1 O  Me        H         H                                    1235                                                                               tetrahydropyrimidin-                                                                      2 1 O  Bn        H         H                                        2-ylamino                                                                  1236                                                                               tetrahydropyrimidin-                                                                      3 1 O  Bn        H         H                                        2-ylamino                                                                  1237                                                                               imidazolin-2-ylamino                                                                      2 1 S  Me        H         H                                    1238                                                                               tetrahydropyrimidin-                                                                      2 1 S  Bn        H         H                                        2-ylamino                                                                  1239                                                                               imidazolin-2-ylamino                                                                      2 1 O  Me        NHCbz     H                                    1240                                                                               tetrahydropyrimidin-                                                                      2 1 O  Me        NHCbz     H                                        2-ylamino                                                                  1241                                                                               imidazolin-2-ylamino                                                                      2 1 O  H         NHCbz     H                                    1242                                                                               tetrahydropyrimidin-                                                                      2 1 O  H         NHCbz     H                                        2-ylamino                                                                  1243                                                                               imidazolin-2-ylamino                                                                      3 1 O  H         NHCbz     H                                    1244                                                                               tetrahydropyrimidin-                                                                      3 1 O  H         NHCbz     H                                        2-ylamino                                                                  1245                                                                               pyridin-2-ylamino                                                                         2 1 O  H         NHCbz     H                                    1246                                                                               imidazol-2-ylamino                                                                        2 1 O  H         NHCbz     H                                    1251                                                                               benzimidazol-2-                                                                           2 1 O  H         NHCbz     H                                        ylamino                                                                    1252                                                                               benzthiazol-2-                                                                            2 1 O  H         NHCbz     H                                        ylamino                                                                    1255                                                                               imidazol-4-ylamino                                                                        2 1 O  H         NHCbz     H                                    1262                                                                               pyridin-2-ylamino                                                                         3 0 O  H         NHCbz     H                                    1263                                                                               imidazol-2-ylamino                                                                        3 0 O  H         NHCbz     H                                    1268                                                                               benzimidazol-2-                                                                           3 0 O  H         NHCbz     H                                        ylamino                                                                    1269                                                                               benzthiazol-2-                                                                            3 0 O  H         NHCbz     H                                        ylamino                                                                    1272                                                                               imidazol-4-ylamino                                                                        3 0 O  H         NHCbz     H                                    1279                                                                               pyridin-2-ylamino                                                                         2 0 O  H         NHCbz     H                                    1280                                                                               imidazol-2-ylamino                                                                        2 0 O  H         NHCbz     H                                    1285                                                                               benzimidazol-2-                                                                           2 0 O  H         NHCbz     H                                        ylamino                                                                    1286                                                                               benzthiazol-2-                                                                            2 0 O  H         NHCbz     H                                        ylamino                                                                    1289                                                                               imidazol-4-ylamino                                                                        2 0 O  H         NHCbz     H                                    1297                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 -n-Bu                                                                         H  447.5                             1298                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2 Ph                                                                            H  481.4                             1299                                                                               imidazolin-2-ylamino                                                                      2 0 O  H         NHSO.sub.2 Ph                                                                            H  467.3                             1300                                                                               imidazolin-2-ylamino                                                                      3 0 O  H         NHSO.sub.2  4-(3,5-                                                                      H  500.3                                                             dimethyl)                                                                      isoxazolyl!                                    1301                                                                               5-nitropyridin-2-                                                                         3 0 O  H         NHCbz     H  498.2                                 ylamino                                                                    1302                                                                               imidazol-2-ylamino                                                                        3 0 O  H         NHSO.sub.2 (2,4,6-                                                                       H                                                                    trimethylphenyl)                               1303                                                                               imidazol-2-ylamino                                                                        3 0 O  H         NHSO.sub.2 (2,4,6-                                                                       H                                                                    trichlorophenyl)                               1304                                                                               imidazol-2-ylamino                                                                        3 0 0  H         NHSO.sub.2 (2,6-                                                                         H                                                                    dichlorophenyl)                                1305                                                                               imidazol-2-ylamino                                                                        3 0 O  H         NHSO.sub.2 (2-chloro-6-                                                                  H                                                                    methylphenyl)                                  1306                                                                               imidazol-2-ylamino                                                                        3 0 O  H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)                                                  H                                    1307                                                                               imidazol-2-ylamino                                                                        3 0 O  H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                                                        H                                    1308                                                                               imidazol-2-ylamino                                                                        3 0 O  H         NHSO2 4-(2,6-                                                                            H                                                                    dimethylphenyl)phenyl                          1309                                                                               imidazol-2-ylamino                                                                        3 0 O  H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                                                        H                                    1310                                                                               imidazol-2-ylamino                                                                        3 0 O  H         NHSO.sub.2  4-(3,5-                                                                      H                                                                    dimethyl)isoxazolyl!                           1311                                                                               imidazol-2-ylamino                                                                        3 0 O  H         NHSO.sub.2 (1-napthyl)                                                                   H                                    1312                                                                               imidazol-2-ylamino                                                                        3 0 O  H         NHSO.sub.2 (2-napthyl)                                                                   H                                    1313                                                                               imidazol-2-ylamino                                                                        3 0 O  H         NHSO.sub.2 NHCH.sub.2 Ph                                                                 H                                    1314                                                                               imidazol-2-ylamino                                                                        3 0 O  H         NHSO.sub.2 NHPh                                                                          H                                    1315                                                                               imidazol-2-ylamino                                                                        3 0 O  Ph        H         H                                    1316                                                                               imidazol-2-ylamino                                                                        3 0 O  phenylsulfonyl-                                                                          H         H                                                          aminomethyl                                              1317                                                                               imidazol-2-ylamino                                                                        3 0 0  3-        H         H                                                          azabicyclo  3.2.2!                                                             nonan-3-                                                                       ylcarbonyl                                               1318                                                                               imidazol-2-ylamino                                                                        3 0 O  adamantan-1-                                                                             H         H                                                          yl                                                                             methylaminocarbonyl                                      1319                                                                               imidazol-2-ylamino                                                                        3 0 O  adamantan-1-                                                                             H         H                                                          yl                                                                             aminocarbonyl                                            1320                                                                               imidazol-2-ylamino                                                                        3 0 O  adamantan-2-                                                                             H         H                                                          yl                                                                             aminocarbonyl                                            1321                                                                               imidazol-2-ylamino                                                                        3 0 O  tetrahydroisoquinolin-                                                                   H         H                                                          2-ylcarbonyl                                             1322                                                                               imidazol-2-                                                                               2 0 O  H         NHSO.sub.2 (2,4,6-                                                                       H                                        ylaminocarbonyl             trimethylphenyl)                               1323                                                                               imidazol-2-                                                                               2 0 O  H         NHSO.sub.2 (2,4,6-                                                                       H                                        ylaminocarbonyl             trichlorophenyl)                               1324                                                                               imidazol-2-                                                                               2 0 O  H         NHSO.sub.2 (2,6-                                                                         H                                        ylaminocarbonyl             dichlorophenyl)                                1325                                                                               imidazol-2-                                                                               2 0 O  H         NHSO.sub.2 (2-chloro-6-                                                                  H                                        ylaminocarbonyl             methylphenyl)                                  1326                                                                               imidazol-2-                                                                               2 0 O  H         NHSO.sub.2 C.sub.6 H.sub.4 (2-CH.sub.3)                                                  H                                        ylaminocarbonyl                                                            1327                                                                               imidazol-2-                                                                               2 0 O  H         NHSO.sub.2 C.sub.6 H.sub.4 (2-Br)                                                        H                                        ylaminocarbonyl                                                            1328                                                                               imidazol-2-                                                                               2 0 O  H         NHSO.sub.2  4-(2,6-                                                                      H                                        ylaminocarbonyl             dimethylphenyl)phenyl                          1329                                                                               imidazol-2-                                                                               2 0 O  H         NHSO.sub.2 C.sub.6 H.sub.4 (4-Ph)                                                        H                                        ylaminocarbonyl                                                            1330                                                                               imidazol-2-                                                                               2 0 O  H         NHSO.sub.2  4-(3,5-                                                                      H                                        ylaminocarbonyl             dimethyl)isoxazolyl!                           1331                                                                               imidazol-2-                                                                               2 0 O  H         NHSO.sub.2 (1-napthyl)                                                                   H                                        ylaminocarbonyl                                                            1332                                                                               imidazol-2-                                                                               2 0 O  H         NHSO.sub.2 (2-napthyl)                                                                   H                                        ylaminocarbonyl                                                            1333                                                                               imidazol-2-                                                                               2 0 O  H         NHSO.sub.2 NHCH.sub.2 Ph                                                                 H                                        ylaminocarbonyl                                                            1334                                                                               imidazol-2-                                                                               2 0 O  H         NHSO.sub.2 NHPh                                                                          H                                        ylaminocarbonyl                                                            __________________________________________________________________________

                  TABLE 4                                                          ______________________________________                                          ##STR37##                                                                     NO.  R.sup.1U  V          Q    R.sup.8                                                                            R.sup.9                                                                             MS                                     ______________________________________                                         1501 imidazolin-                                                                              1,4-phenylene                                                                             O    H   NHCBz                                            2-ylamino                                                                 1502 tetrahydro-                                                                              1,4-phenylene                                                                             O    H   NHCBz                                            pyrimidin-                                                                     2-ylamino                                                                 1503 imidazolin-                                                                              1,4-phenylene                                                                             O    H   NHSO.sub.2 -n-Bu                                 2-ylamino                                                                 1504 tetrahydro-                                                                              1,4-phenylene                                                                             O    H   NHSO.sub.2 -n-Bu                                 pyrimidin-                                                                     2-ylamino                                                                 1505 imidazolin-                                                                              1,4-phenylene                                                                             S    H   NHCbz                                            2-ylamino                                                                 1506 tetrahydro-                                                                              1,4-phenylene                                                                             S    H   NHCbz                                            pyrimidin-                                                                     2-ylamino                                                                 1507 imidazolin-                                                                              1,4-phenylene                                                                             S    H   NHSO.sub.2 -n-Bu                                 2-ylamino                                                                 1508 tetrahydro-                                                                              1,4-phenylene                                                                             S    H   NHSO.sub.2 -n-Bu                                 pyrimidin-                                                                     2-ylamino                                                                 1509 imidazolin-                                                                              1,4-phenylene                                                                             NH   H   NHCbz                                            2-ylamino                                                                 1510 tetrahydro-                                                                              1,4-phenylene                                                                             NH   H   NHCbz                                            pyrimidin-                                                                     2-ylamino                                                                 1511 imidazolin-                                                                              1,4-phenylene                                                                             NH   H   NHSO.sub.2 -n-Bu                                 2-ylamino                                                                 1512 tetrahydro-                                                                              1,4-phenylene                                                                             NH   H   NHSO.sub.2 -n-Bu                                 pyrimidin-                                                                     2-ylamino                                                                 1513 imidazolin-                                                                              1,4-phenylene                                                                             O    Me  H                                                2-ylamino                                                                 1514 tetrahydro-                                                                              1,4-phenylene                                                                             O    Me  H                                                pyrimidin-                                                                     2-ylamino                                                                 1515 imidazolin-                                                                              1,4-phenylene                                                                             O    Bn  H                                                2-ylamino                                                                 1516 tetrahydro-                                                                              1,4-phenylene                                                                             O    Bn  H                                                pyrimidin-                                                                     2-ylamino                                                                 1517 imidazolin-                                                                              1,4-phenylene                                                                             S    Me  H                                                2-ylamino                                                                 1518 tetrahydro-                                                                              1,4-phenylene                                                                             S    Me  H                                                pyrimidin-                                                                     2-ylamino                                                                 1519 imidazolin-                                                                              1,4-phenylene                                                                             S    Bn  H                                                2-ylamino                                                                 1520 tetrahydro-                                                                              1,4-phenylene                                                                             S    Bn  H                                                pyrimidin-                                                                     2-ylamino                                                                 1521 imidazolin-                                                                              1,4-phenylene                                                                             O    Me  NHCbz                                            2-ylamino                                                                 1522 tetrahydro-                                                                              1,4-phenylene                                                                             O    Me  NHCbz                                            pyrimidin-                                                                     2-ylamino                                                                 1523 imidazolin-                                                                              1,4-phenylene                                                                             O    H   NHCbz                                            2-ylamino                                                                 1524 tetrahydro-                                                                              1,4-phenylene                                                                             O    H   NHCbz                                            pyrimidin-                                                                     2-ylamino                                                                 1525 imidazolin-                                                                              1,3-phenylene                                                                             O    H   NHCbz                                            2-ylamino                                                                 1526 tetrahydro-                                                                              1,3-phenylene                                                                             O    H   NHCbz                                            pyrimidin-                                                                     2-ylamino                                                                 1527 imidazolin-                                                                              1,3-phenylene                                                                             O    H   NHSO.sub.2 -n-Bu                                 2-ylamino                                                                 1528 tetrahydro-                                                                              1,3-phenylene                                                                             O    H   NHSO.sub.2 -n-Bu                                 pyrimidin-                                                                     2-ylamino                                                                 1529 imidazolin-                                                                              1,3-phenylene                                                                             S    H   NHCbz                                            2-ylamino                                                                 1530 tetrahydro-                                                                              1,3-phenylene                                                                             S    H   NHCbz                                            pyrimidin-                                                                     2-ylamino                                                                 1531 imidazolin-                                                                              1,3-phenylene                                                                             S    H   NHSO.sub.2 -n-Bu                                 2-ylamino                                                                 1532 tetrahydro-                                                                              1,3-phenylene                                                                             S    H   NHSO.sub.2 -n-Bu                                 pyrimidin-                                                                     2-ylamino                                                                 1533 imidazolin-                                                                              1,3-phenylene                                                                             NH   H   NHCbz                                            2-ylamino                                                                 1534 tetrahydro-                                                                              1,3-phenylene                                                                             NH   H   NHCbz                                            pyrimidin-                                                                     2-ylamino                                                                 1535 imidazolin-                                                                              1,3-phenylene                                                                             NH   H   NHCbz                                            2-ylamino                                                                 1536 tetrahydro-                                                                              1,3-phenylene                                                                             NH   H   NHCbz                                            pyrimidin-                                                                     2-ylamino                                                                 1537 imidazolin-                                                                              1,3-phenylene                                                                             O    Me  H                                                2-ylamino                                                                 1538 tetrahydro-                                                                              1,3-phenylene                                                                             O    Me  H                                                pyrimidin-                                                                     2-ylamino                                                                 1539 imidazolin-                                                                              1,3-phenylene                                                                             O    Bn  H                                                2-ylamino                                                                 1540 tetrahydro-                                                                              1,3-phenylene                                                                             O    Bn  H                                                pyrimidin-                                                                     2-ylamino                                                                 1541 imidazolin-                                                                              1,3-phenylene                                                                             O    Me  NHCbz                                            2-ylamino                                                                 1542 tetrahydro-                                                                              1,3-phenylene                                                                             O    Me  NHCbz                                            pyrimidin-                                                                     2-ylamino                                                                 1543 imidazolin-                                                                              1,3-phenylene                                                                             S    Me  H                                                2-ylamino                                                                 1544 tetrahydro-                                                                              1,3-phenylene                                                                             S    Me  H                                                pyrimidin-                                                                     2-ylamino                                                                 1545 imidazolin-                                                                              1,3-phenylene                                                                             S    Bn  H                                                2-ylamino                                                                 1546 tetrahydro-                                                                              1,3-phenylene                                                                             S    Bn  H                                                pyrimidin-                                                                     2-ylamino                                                                 1547 imidazolin-                                                                              1,3-phenylene                                                                             O    H   NHCbz                                            2-ylamino                                                                 1548 tetrahydro-                                                                              1,3-phenylene                                                                             O    H   NHCbz                                            pyrimidin-                                                                     2-ylamino                                                                 ______________________________________                                    

                  TABLE 5                                                          ______________________________________                                          ##STR38##                                                                     NO.  R.sup.1U      m      Q    R.sup.8 R.sup.14                                                                            MS                                 ______________________________________                                         1601 imidazolin-2-ylamino                                                                         2      O    Bn      H                                       1602 imidazolin-2-ylamino                                                                         3      O    Bn      H                                       1603 tetrahydropyrimidin-                                                                         2      O    Bn      H                                            2-ylamino                                                                 1604 tetrahydropyrimidin-                                                                         3      O    Bn      H                                            2-ylamino                                                                 1605 imidazolin-2-ylamino                                                                         2      O    Bn(p-OCH.sub.3)                                                                        H                                       1606 tetrahydropyrimidin-                                                                         2      O    Bn(p-OCH.sub.3)                                                                        H                                            2-ylamino                                                                 1607 imidazolin-2-ylamino                                                                         3      O    Bn(p-OCH.sub.3)                                                                        H                                       1608 tetrahydropyrimidin-                                                                         3      O    Bn(p-OCH.sub.3)                                                                        H                                            2-ylamino                                                                 1609 imidazolin-2-ylamino                                                                         2      O    Bn(p-F) H                                       1610 imidazolin-2-ylamino                                                                         3      O    Bn(p-F)                                         1611 tetrahydropyrimidin-                                                                         2      O    Bn(p-F) H                                            2-ylamino                                                                 1612 tetrahydropyrimidin-                                                                         3      O    Bn(p-F) H                                            2-ylamino                                                                 1613 imidazolin-2-ylamino                                                                         2      S    Bn      H                                       1614 imidazolin-2-ylamino                                                                         3      S    Bn      H                                       1615 tetrahydropyrimidin-                                                                         2      S    Bn      H                                            2-ylamino                                                                 1616 tetrahydropyrimidin-                                                                         3      S    Bn      H                                            2-ylamino                                                                 1617 imidazolin-2-ylamino                                                                         2      O    Bn      Me                                      1618 imidazolin-2-ylamino                                                                         3      O    Bn      Me                                      1619 tetrahydropyrimidin-                                                                         2      O    Bn      Me                                           2-ylamino                                                                 1620 tetrahydropyrimidin-                                                                         3      O    Bn      Me                                           2-ylamino                                                                 1621 imidazolin-2-ylamino                                                                         2      NH   Bn      H                                       1622 imidazolin-2-ylamino                                                                         3      NH   Bn      H                                       1623 tetrahydropyrimidin-                                                                         2      NH   Bn      H                                            2-ylamino                                                                 1624 tetrahydropyrimidin-                                                                         3      NH   Bn      H                                            2-ylamino                                                                 ______________________________________                                    

Utility

The compounds of Formula I of the present invention possess activity as antagonists of integrins such as, for example, the α_(v) β₃ or vitronectin receptor, α_(v) β₅ or α₅ β1, and as such have utility in the treatment and diagnosis of cell adhesion, angiogenic disorders, inflammation, bone degradation, cancer metastases, diabetic retinopathy, thrombosis, restenosis, macular degeneration, and other conditions mediated by cell adhesion and/or cell migration and/or angiogenesis. The integrin antagonist activity of the compounds of the present invention is demonstrated using assays which measure the binding of a specific integrin to a native ligand, for example, using the ELISA assay described below for the binding of vitronectin to the α_(v) β₃ receptor.

The compounds of the present invention possess selectivity for the α_(v) β₃ receptor relative to the GPIIb/IIIa receptor as demonstrated by their lack of activity in standard assays of platelet aggregation, such as the platelet aggregation assay described below.

One of the major roles of integrins in vivo is to mediate cellular interactions with adjacent cells. Cell based adhesion assays can be used to mimic these interactions in vitro. A cell based assay is more representative of the in vivo situation than an ELISA since the receptor is maintained in membranes in the native state. The compounds of the present invention have activity in cell-based assays of adhesion, for example as demonstrated in using the cell adhesion assays described below.

The compounds of Formula I of the present invention may be useful for the treatment or prevention of other diseases which involve cell adhesion processes, including, but not limited to, osteoporosis, rheumatoid arthritis, autoimmune disorders, bone degradation, rheumatoid arthritis, asthma, allergies, adult respiratory distress syndrome, graft versus host disease, organ transplantation, septic shock, psoriasis, eczema, contact dermatitis, osteoarthritis, atherosclerosis, metastasis, wound healing, inflammatory bowel disease and other angiogenic disorders.

The compounds of Formula I have the ability to suppress/inhibit angiogenesis in vivo, for example, as demonstrated using animal models of ocular neovascularization.

The compounds provided by this invention are also useful as standards and reagents in determining the ability of a potential pharmaceutical to inhibit integrin-ligand binding. These may be provided in a commercial kit comprising a compound of this invention.

As used herein "μg" denotes microgram, "mg" denotes milligram, "g" denotes gram, "μL" denotes microliter, "mL" denotes milliliter, "L" denotes liter, "nM" denotes nanomolar, "μM" denotes micromolar, "mM" denotes millimolar, "M" denotes molar and "nm" denotes nanometer. "Sigma" stands for the Sigma-Aldrich Corp. of St. Louis, Mo.

The utility of the compounds of the present invention may be assessed by testing in one or more of the following assays as described in detail below: Purified α_(v) β₃ (human placenta)--Vitronectin ELISA, α_(v) β₃ -Vitronectin Binding Assay, Human Aortic Smooth Muscle Cell Migration Assay, In Vivo Angiogenesis Model, Pig Restenosis Model, Mouse Retinopathy Model. A compound of the present invention is considered to be active if it has an IC₅₀ or K_(i) value of less than about 10 μM for the inhibition of α_(v) β₃ -Vitronectin Binding Assay, with compounds preferably having K_(i) values of less than about 0.1 μM. Tested compounds of the present invention are active in the α_(v) β₃ -Vitronectin Binding Assay.

Purified α_(v) β₃ (human placenta)--Vitronectin ELISA

The α_(v) β₃ receptor was isolated from human placental extracts prepared using octylglucoside. The extracts were passed over an affinity column composed of anti-α_(v) β₃ monoclonal antibody (LM609) to Affigel. The column was subsequently washed extensively at pH 7 and pH 4.5 followed by elution at pH 3. The resulting sample was concentrated by wheat germ agglutinin chromatography to provide gave two bands on SDS gel which were confirmed as α_(v) β₃ by western blotting.

Affinity purified protein was diluted at different levels and plated to 96 well plates. ELISA was performed using fixed concentration of biotinylated vitronectin (approximately 80 nM/well). This receptor preparation contains the α_(v) β₃ with no detectable levels of α_(v) β₅ according to the gel (α_(v) β₃) and according to effects of blocking antibodies for the α_(v) β₃ or α_(v) β₅ in the ELISA.

A submaximal concentration of biotinylated vitronectin was selected based on conc. response curve with fixed receptor conc. and variable concentrations of biotinylated vitronectin.

α_(v) β₃ -Vitronectin Binding Assay

The purified receptor is diluted with coating buffer (20 mM Tris HCl, 150 mM NaCl, 2.0 mM CaCl₂, 1.0 mM MgCl₂.6H₂ O, 1.0 mM MnCl₂.4H₂ O) and coated (100 μL/well) on Costar (3590) high capacity binding plates overnight at 4° C. The coating solution is discarded and the plates washed once with blocking/binding buffer (B/B buffer, 50 mM Tris HCl, 100 mM NaCl, 2.0 mM CaCl₂, 1.0 mM MgCl₂.6H₂ O, 1.0 mM MnCl₂.4H₂ O). Receptor is then blocked (200 μL/well) with 3.5% BSA in B/B buffer for 2 hours at room temperature. After washing once with 1.0% BSA in B/B buffer, biotinylated vitronectin (100 μL) and either inhibitor (11 μL) or B/B buffer w/1.0% BSA (11 μL) is added to each well. The plates are incubated 2 hours at room temperature. The plates are washed twice with B/B buffer and incubated 1 hour at room temperature with anti-biotin alkaline phosphatase (100 μL/well) in B/B buffer containing 1.0% BSA. The plates are washed twice with B/B buffer and alkaline phosphatase substrate (100 μL) is added. Color is developed at room temperature. Color development is stopped by addition of 2N NaOH (25 μL/well) and absorbance is read at 405 nm. The IC₅₀ is the concentration of test substance needed to block 50% of the vitronectin binding to the receptor.

Integrin Cell-Based Adhesion Assays

In the adhesion assays, a 96 well plate was coated with the ligand (i.e., fibrinogen) and incubated overnight at 4° C. The following day, the cells were harvested, washed and loaded with a fluorescent dye. Compounds and cells were added together and then were immediately added to the coated plate. After incubation, loose cells are removed from the plate, and the plate (with adherent cells) is counted on a fluorometer. The ability of test compounds to inhibit cell adhesion by 50% is given by the IC₅₀ value and represents a measure of potency of inhibition of integrin mediated binding. Compounds were tested for their ability to block cell adhesion using assays specific for α_(v) β₃, α_(v) β5 and α₅ β₁ integrin interactions.

Platelet Aggregation Assay

Venous blood was obtained from anesthetized mongrel dogs or from healthy human donors who were drug- and aspirin-free for at least two weeks prior to blood collection. Blood was collected into citrated Vacutainer tubes. The blood was centrifuged for 15 minutes at 150×g (850 RPM in a Sorvall RT6000 Tabletop Centrifuge with H-1000 B rotor) at room temperature, and platelet-rich plasma (PRP) was removed. The remaining blood was centrifuged for 15 minutes at 1500×g (26,780 RPM) at room temperature, and platelet-poor plasma (PPP) was removed. Samples were assayed on a PAP-4 Platelet Aggregation Profiler, using PPP as the blank (100% transmittance). 200 μL of PRP (5×10⁸ platelets/mL) were added to each micro test tube, and transmittance was set to 0%. 20 μL of ADP (10 μM) was added to each tube, and the aggregation profiles were plotted (% transmittance versus time). Test agent (20 μL) was added at different concentrations prior to the addition of the platelet agonist. Results are expressed as % inhibition of agonist-induced platelet aggregation.

Human Aortic Smooth Muscle Cell Migration Assay

A method for assessing α_(v) β₃ -mediated smooth muscle cell migration and agents which inhibit α_(v) β₃ -mediated smooth muscle cell migration is described in Liaw et al., J. Clin. Invest. (1995) 95: 713-724).

In Vivo Angiogenesis Model

A quantitative method for assessing angiogenesis and antiangiogenic agents is described in Passaniti et al., Laboratory Investigation (1992) 67:519-528

Pig Restenosis Model

A method for assessing restenosis and agents which inhibit restenosis is described in Schwartz et al., J. Am. College of Cardiology (1992) 19: 267-274.

Mouse Retinopathy Model

A method for assessing retinopathy and agents which inhibit retinopathy is described in Smith et al., Invest. Ophthal. & Visual Science (1994) 35: 101-111.

Dosage and Formulation

The compounds of this invention can be administered by any means that produces contact of the active agent with the agent's site of action, the α_(v) β₃ integrin, in the body of a mammal. They can be administered by any conventional means available for use in conjunction with pharmaceuticals, either as individual therapeutic agents or in a combination of therapeutic agents, such as a antiplatelet agent such as aspirin, piroxicam, or ticlopidine which are agonist-specific, or an anti-coagulant such as warfarin or heparin, or a thrombin inhibitor such as a boropeptide, hirudin or argatroban, or a thrombolytic agent such as tissue plasminogen activator, anistreplase, urokinase or streptokinase, or combinations thereof. The compounds of the invention, or compounds of the invention in combination with other therapeutic agents, can be administered alone, but generally administered with a pharmaceutical carrier selected on the basis of the chosen route of administration and standard pharmaceutical practice.

The dosage of the novel cyclic compounds of this invention administered will, of course, vary depending upon known factors, such as the pharmacodynamic characteristics of the particular agent and its mode and route of administration; the age, health and weight of the recipient; the nature and extent of the symptoms; the kind of concurrent treatment; the frequency of treatment; and the effect desired. A daily dosage of active ingredient can be expected to be about 0.001 to 10 milligrams per kilogram of body weight.

Dosage forms (compositions suitable for administration) contain from about 0.1 milligram to about 100 milligrams of active ingredient per unit. In these pharmaceutical compositions the active ingredient will ordinarily be present in an amount of about 0.5-95% by weight based on the total weight of the composition.

The active ingredient can be administered orally in solid dosage forms, such as capsules, tablets, and powders, or in liquid dosage forms, such as elixirs, syrups, and suspensions. It can also be administered parenterally, in sterile liquid dosage forms.

Gelatin capsules contain the active ingredient and powdered carriers, such as lactose, starch, cellulose derivatives, magnesium stearate, stearic acid, and the like. Similar diluents can be used to make compressed tablets. Both tablets and capsules can be manufactured as sustained release products to provide for continuous release of medication over a period of hours. Compressed tablets can be sugar coated or film coated to mask any unpleasant taste and protect the tablet from the atmosphere, or enteric coated for selective disintegration in the gastrointestinal tract.

Liquid dosage forms for oral administration can contain coloring and flavoring to increase patient acceptance.

In general, water, a suitable oil, saline, aqueous dextrose (glucose), and related sugar solutions and glycols such as propylene glycol or polyethylene glycols are suitable carriers for parenteral solutions. Solutions for parenteral administration preferably contain a water soluble salt of the active ingredient, suitable stabilizing agents, and if necessary, buffer substances. Antioxidizing agents such as sodium bisulfite, sodium sulfite, or ascorbic acid, either alone or combined, are suitable stabilizing agents. Also used are citric acid and its salts and sodium EDTA. In addition, parenteral solutions can contain preservatives, such as benzalkonium chloride, methyl- or propyl-paraben, and chlorobutanol.

Suitable pharmaceutical carriers are described in Remington's Pharmaceutical Sciences, Mack Publishing Company, a standard reference text in this field.

Useful pharmaceutical dosage-forms for administration of the compounds of this invention can be illustrated as follows:

Capsules

A large number of unit capsules are prepared by filling standard two-piece hard gelatin capsules each with 10 milligrams of powdered active ingredient, 150 milligrams of lactose, 50 milligrams of cellulose, and 6 milligrams magnesium stearate.

Soft Gelatin Capsules

A mixture of active ingredient in a digestable oil such as soybean oil, cottonseed oil or olive oil is prepared and injected by means of a positive displacement pump into gelatin to form soft gelatin capsules containing 10 milligrams of the active ingredient. The capsules are washed and dried.

Tablets

A large number of tablets are prepared by conventional procedures so that the dosage unit was 10 milligrams of active ingredient, 0.2 milligrams of colloidal silicon dioxide, 5 milligrams of magnesium stearate, 275 milligrams of microcrystalline cellulose, 11 milligrams of starch and 98.8 milligrams of lactose. Appropriate coatings may be applied to increase palatability or delay absorption.

The compounds for the present invention can be administered in intranasal form via topical use of suitable intranasal vehicles, or via transdermal routes, using those forms of transdermal skin patches wall known to those of ordinary skill in that art. To be administered in the form of a transdermal delivery system, the dosage administration will, of course, be continuous rather than intermittant throughout the dosage regimen.

The active ingredient can be administered intranasally to a mammal at a dosage range of about 0.01 to 0.5 mg/kg while the preferred dosage range is about 0.01-0.1 mg/kg.

Compositions of the active ingredients can be administered intranasally by preparing a suitable formulation of the active ingredient by procedures well known to those skilled in the art. Preferably the formulations are prepared with suitable nontoxic pharmaceutically acceptable ingredients. These ingredients are known to those skilled in the preparation of nasal dosage forms and some of these can be found in REMINGTON'S PHARMACEUTICAL SCIENCES. 17th edition, 1985 a standard reference in the field. The choice of suitable carriers is highly dependent upon the exact nature of the nasal dosage form desired, e.g., solutions, suspensions, ointments, or gels. Nasal dosage forms generally contain large amounts of water in addition to the active ingredient. Minor amounts of other ingredients such as pH adjusters, emulsifiers or dispersing agents, preservatives, surfactants, jelling agents, or buffering and other stabilizing and solubilizing agents may also be present. Preferably, the nasal dosage form should be isotonic with nasal secretions.

An example of a nasal solution composition of this invention includes:

    ______________________________________                                         Active Drug           0.2-2 g                                                  Sorbitol              0.6 g                                                    Benzalkonium chloride 0.002 g                                                  Hydrochloric acid     to adjust pH                                             Sodium hydroxide      to adjust pH                                             Purified water        to 10 mL                                                 ______________________________________                                    

In this example the active drug can be in one vial and the rest of the formulation can be in another vial. The drug can be reconstituted when needed.

The formulation of this invention may be varied to include: (1) other acids and bases to adjust the pH; (2) other tonicity imparting agents such as glycerin and dextrose; (3) other antimicrobial preservatives such as other parahydroxy benzoic acid esters, sorbate, benzoate, propionate, chlorbutanol, phenylethyl alcohol, and mercurials; (4) other viscosity imparting agents such as sodium carboxy-methylcellulose microcrystalline cellulose, polyvinyl-pyrrolidone, polyvinyl alcohol and other gums; (5) suitable absorption enhancers; (6) stabilizing agents such as antioxidants, like bisulfite and ascorbate, metal chelating agents such as sodium edetate and drug solubility enhancers such as polyethylene glycols.

The above formulation can be administered as drops, sprays, aerosols or by any other intranasal dosage form. Optionally, the delivery system can be a unit dose delivery system. The volume of solution or suspension delivered per dose can be anywhere from 5 to 400 μL, and preferably between 50 and 150 μL. Delivery systems for these various dosage forms can be dropper bottles, plastic squeeze units, atomizers, nebulizers or pharmaceutical aerosols in either unit dose or multiple dose packages.

The combination products of this invention, such as the novel α_(v) β₃ antagonist compounds of this invention in combination with an anti-coagulant agent such as warfarin or heparin, or an anti-platelet agent such as aspirin, piroxicam or ticlopidine, or a thrombin inhibitor such as a boropeptide, hirudin or argatroban, or a thrombolytic agent such as tissue plasminogen activator, anistreplase, urokinase or streptokinase, or combinations thereof, can be in any dosage form, such as those described above, and can also be administered in various ways, as described above.

In a preferred embodiment, the combination products of the invention are formulated together, in a single dosage form (that is, combined together in one capsule, tablet, powder, or liquid, etc.). When the combination products are not formulated together in a single dosage form, the α_(v) β₃ antagonist compounds of this invention and the anti-coagulant agent, anti-platelet agent, thrombin inhibitor, and/or thrombolytic agent may be administered at the same time (that is, together), or in any order, for example the compounds of this invention are administered first, followed by administration of the anti-coagulant agent, anti-platelet agent, thrombin inhibitor, and/or thrombolytic agent. When not administered at the same time, preferably the administration of the compound of this invention and any anti-coagulant agent, anti-platelet agent, thrombin inhibitor, and/or thrombolytic agent occurs less than about one hour apart, more preferably less than about 30 minutes apart, even more preferably less than about 15 minutes apart, and most preferably less than about 5 minutes apart. Preferably, administration of the combination products of the invention is oral. The terms oral agent, oral inhibitor, oral compound, or the like, as used herein, denote compounds which may be orally administered. Although it is preferable that the α_(v) ↑₃ antagonist compounds of this invention and the anti-coagulant agent, anti-platelet agent, thrombin inhibitor, and/or thrombolytic agent are both administered in the same fashion (that is, for example, both orally), if desired, they may each be administered in different fashions (that is, for example, one component of the combination product may be administered orally, and another component may be administered intravenously). The dosage of the combination products of the invention may vary depending upon various factors such as the pharmacodynamic characteristics of the particular agent and its mode and route of administration, the age, health and weight of the recipient, the nature and extent of the symptoms, the kind of concurrent treatment, the frequency of treatment, and the effect desired, as described above.

As discussed above, where two or more of the foregoing therapeutic agents are combined or co-administered with the compounds of this invention, generally the amount of each component in a typical daily dosage and typical dosage form may be reduced relative to the usual dosage of the agent when administered alone, in view of the additive or synergistic effect which would be obtained as a result of addition of further agents in accordance with the present invention.

Particularly when provided as a single dosage form, the potential exists for a chemical interaction between the combined active ingredients (for example, a novel compound of this invention and an anti-coagulant such as warfarin or heparin, or a novel compound of this invention and an anti-platelet agent such as aspirin, piroxicam or ticlopidine, or a novel compound of this invention and a thrombin inhibitor such as a boropeptide, hirudin or argatroban, or a novel compound of this invention and a thrombolytic agent such as tissue plasminogen activator, anistreplase, urokinase or streptokinase, or combinations thereof). For this reason, the preferred dosage forms of the combination products of this invention are formulated such that although the active ingredients are combined in a single dosage form, the physical contact between the active ingredients is minimized (that is, reduced).

In order to minimize contact, one embodiment of this invention where the product is orally administered provides for a combination product wherein one active ingredient is enteric coated. By enteric coating one of the active ingredients, it is possible not only to minimize the contact between the combined active ingredients, but also, it is possible to control the release of one of these components in the gastrointestinal tract such that one of these components is not released in the stomach but rather is released in the intestines. Another embodiment of this invention where oral administration is desired provides for a combination product wherein one of the active ingredients is coated with a sustained-release material which effects a sustained-release throughout the gastrointestinal tract and also serves to minimize physical contact between the combined active ingredients. Furthermore, the sustained-released component can be additionally enteric coated such that the release of this component occurs only in the intestine. Still another approach would involve the formulation of a combination product in which the one component is coated with a sustained and/or enteric release polymer, and the other component is also coated with a polymer such as a low viscosity grade of hydroxypropyl methylcellulose (HPMC) or other appropriate materials as known in the art, in order to further separate the active components. The polymer coating serves to form an additional barrier to interaction with the other component.

Dosage forms of the combination products of the present invention wherein one active ingredient is enteric coated can be in the form of tablets such that the enteric coated component and the other active ingredient are blended together and then compressed into a tablet or such that the enteric coated component is compressed into one tablet layer and the other active ingredient is compressed into an additional layer. Optionally, in order to further separate the two layers, one or more placebo layers may be present such that the placebo layer is between the layers of active ingredients. In addition, dosage forms of the present invention can be in the form of capsules wherein one active ingredient is compressed into a tablet or in the form of a plurality of microtablets, particles, granules or non-perils, which are then enteric coated. These enteric coated microtablets, particles, granules or non-perils are then placed into a capsule or compressed into a capsule along with a granulation of the other active ingredient.

These as well as other ways of minimizing contact between the components of combination products of the present invention, whether administered in a single dosage form or administered in separate forms but at the same time by the same manner, will be readily apparent to those skilled in the art, once armed with the present disclosure.

Pharmaceutical kits useful in, for example, the inhibition of thrombus formation, the prevention of blood clots, and/or the treatment of thromboembolic disorders, which comprise a therapeutically effective amount of a compound according to the method of the present invention along with a therapeutically effective amount of an anti-coagulant agent such as warfarin or heparin, or an anti-platelet agent such as aspirin, piroxicam or ticlopidine, or a thrombin inhibitor such as a boropeptide, hirudin or argatroban, or a thrombolytic agent such as tissue plasminogen activator, anistreplase, urokinase or streptokinase, or combinations thereof, in one or more sterile containers, are also within the ambit of the present invention. Sterilization of the container may be carried out using conventional sterilization methodology well known to those skilled in the art. The sterile containers of materials may comprise separate containers, or one or more multi-part containers, as exemplified by the UNIVIAL™ two-part container (available from Abbott Labs, Chicago, Ill.), as desired. The compounds according to the method of the invention and the anti-coagulant agent, anti-platelet agent, thrombin inhibitor, thrombolytic agent, and/or combinations thereof, may be separate, or combined into a single dosage form as described above. Such kits may further include, if desired, one or more of various conventional pharmaceutical kit components, such as for example, one or more pharmaceutically acceptable carriers, additional vials for mixing the components, etc., as will be readily apparent to those skilled in the art. Instructions, either as inserts or as labels, indicating quantities of the components to be administered, guidelines for administration, and/or guidelines for mixing the components, may also be included in the kit. 

What is claimed is:
 1. A compound of Formula I: ##STR39## including stereoisomeric forms thereof, or mixtures of stereoisomeric forms thereof, or a pharmaceutically acceptable salt thereof wherein:b, the bond between carbon atoms numbered 4 and 5, is a carbon-carbon single or double bond; R¹ is selected from: ##STR40## A and B are independently --CH₂ --, --O--, --N(R¹²)--, or --C(═O)--; A¹ and B¹ are independently --CH₂ -- or --N(R¹⁰)--; D is --N(R^(2a))--, --O--, --S--, --C(═O)-- or --SO₂ --; E--F is --C(R²)═C(R³)--, --N═C(R²)--, --C(R²)═N--, --N═N--, or --C(R²)₂ C(R³)₂ --; J, K, L and M are independently selected from --C(R²)-- or --N--, provided that at least one of J, K, L and M is --C(R²)--; R² and R³ are independently selected from: H, C₁ -C₄ alkoxy, NR¹¹ R¹², ═NR¹², halogen, NO₂, CN, CF₃, C₁ -C₆ alkyl, C₃ -C₆ alkenyl, C₃ -C₇ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, C₆ -C₁₀ aryl, C₇ -C₁₁ arylalkyl, C₂ -C₇ alkylcarbonyl, C₆ -C₁₀ carbonyl or C₇ -C₁₁ arylcarbonyl;alternatively, R² and R³, when substituents on adjacent atoms, are taken together with the carbon atoms to which they are attached to form a 5-7 membered carbocyclic or 5-7 membered heterocyclic aromatic or nonaromatic ring system, said carbocyclic or heterocyclic ring being optionally substituted with 0-2 R⁷ ; R^(2a) is absent or R¹² ; U is selected from:--(CH₂)_(n) --, --(CH₂)_(n) O(CH₂)_(m) --, --(CH₂)_(n) N(R¹²)(CH₂)_(m) --, --(CH₂)_(n) C(═O)(CH₂)_(m) --, --(CH₂)_(n) S(O)_(p) (CH₂)_(m) --, --(CH₂)_(n) NHNH(CH₂)_(m) --, --N(R¹⁰)C(═O)--, or --C(═O)N(R¹⁰)--; --N(R¹⁰)S(O)_(p) --, or V is selected from:--(CH₂)_(n) --, --(C₁ -C₆ alkylene)-Q--, substituted with 0-3 groups independently selected from R¹³, --(C₂ -C₇ alkenylene)-Q--, substituted with 0-3 groups independently selected from R¹³, --(C₂ -C₇ alkynylene)-Q--, substituted with 0-3 groups independently selected from R¹³, -(phenyl)-Q--, said phenyl substituted with 0-2 groups independently selected from R¹³, -(pyridyl)-Q--, said pyridyl substituted with 0-2 groups independently selected from R¹³, or -(pyridazinyl)-Q--, said pyridazinyl substituted with 0-2 groups independently selected from R¹³ ; Q is selected from:--(CH₂)_(n) --, --(CH₂)_(n) O(CH₂)_(m) --, --(CH₂)_(n) N(R¹²)(CH₂)_(m) --, --(CH₂)_(n) C(═O)(CH₂)_(m) --, --(CH₂)_(n) S(O)_(p) (CH₂)_(m) --, --(CH₂)_(n) NHNH(CH₂)_(m) --, --N(R¹⁰)C(═O)--, or --C(═O)N(R¹⁰)--; W is selected from:--(C(R⁴)₂)_(q) C(═O)N(R¹⁰)--, --C(═O)--N(R¹⁰)--(C(R⁴)₂)_(q) --; X is selected from:a single bond, --(C(R⁴)₂)_(q) -- C(R⁴)(R⁸)!_(s) --C(R⁴)(R⁹)--; alternatively, W is ##STR41## and X is absent or --CH₂ --Y is selected from:--COR²⁰ --, --SO₃ H, --PO₃ H, --CONHNHSO₂ CF₃, --CONHSO₂ R^(18a), --CONHSO₂ NHR^(18b), --NHCOCF₃, --NHCONHSO₂ R^(18a), --NHSO₂ R^(18a), --OPO₃ H₂, --OSO₃ H, --PO₃ H₂, --SO₃ H, --SO₂ NHCOR^(18a), --SO₂ NHCO₂ R^(18a), or ##STR42## Z is selected from --CH(R⁹)--, or --N(R¹⁶)--; R⁴ is selected from H, C₁ -C₁₀ alkyl, C₁ -C₁₀ alkylcarbonyl, aryl, arylalkyl, cycloalkyl, or cycloalkylalkyl; alternatively, two R⁴ groups on adjacent carbon atoms join to form a bond, thereby forming a carbon-carbon double or triple bond between the adjacent carbon atoms; R⁵ is selected from H, C₁ -C₆ alkyl, C₂ -C₆ alkenyl, C₂ -C₆ alkynyl, C₃ -C₇ cycloalkyl, C₇ -C₁₄ bicycloalkyl, hydroxy, C₁ -C₆ alkoxy, C₁ -C₆ alkylthio, C₁ -C₆ alkylsulfinyl, C₁ -C₆ alkylsulfonyl, nitro, C₁ -C₆ alkylcarbonyl, C₆ -C₁₀ aryl, --N(R¹¹)R¹², halo, CF₃, CN, C₁ -C₆ alkoxycarbonyl, carboxy, piperidinyl, morpholinyl or pyridinyl; R⁶ is selected from:H, C₁ -C₁₀ alkyl, hydroxy, C₁ -C₁₀ alkoxy, nitro, C₁ -C₁₀ alkylcarbonyl, --N(R¹¹)R¹², cyano, halo, CF₃, CHO, CO₂ R^(18b), C(═O)R^(18b), CONR¹⁷ R^(18b), OC(═O)R¹⁰, OC(═O)OR²¹, OR¹⁰, OC(═O)NR¹⁰ R¹¹, OCH₂ CO₂ R¹⁰, CO₂ CH₂ CO₂ R¹⁰, NO₂, NR¹⁰ C(═O)R¹⁰, NR¹⁰ C(═O)OR²¹, NR¹⁰ C(═O)NR¹⁰ R¹¹, NR¹⁰ SO₂ NR¹⁰ R¹¹, NR¹⁰ SO₂ R²¹, S(O)_(p) R¹¹, SO₂ NR¹⁰ R¹¹, SiMe₃, C₂ to C₆ alkenyl, C₃ to C₁₁ cycloalkyl, C₄ to C₁₁ cycloalkylmethyl, C₆ to C₁₀ aryl optionally substituted with 1-3 groups selected from halogen, C₁ -C₆ alkoxy, C₁ -C₆ alkyl, CF₃, S(O)_(m) Me, or --NMe₂ ; C₇ to C₁₁ arylalkyl, said aryl being optionally substituted with 1-3 groups selected from halogen, C₁ -C₆ alkoxy, C₁ -C₆ alkyl, CF₃, S(O)_(p) Me, or --NMe₂, methylenedioxy when R⁶ is a substituent on aryl, or a 5-10 membered heterocyclic ring containing 1-3 N, O, or S heteroatoms, wherein said heterocyclic ring is saturated, partially saturated, or fully unsaturated, said heterocyclic ring being substituted with 0-2 R⁷ ; R⁷ is selected from:H, C₁ -C₁₀ alkyl, hydroxy, C₁ -C₁₀ alkoxy, nitro, C₁ -C₁₀ alkylcarbonyl, --N(R¹¹) R¹², cyano, halo, CF₃, CHO, CO₂ R¹⁰, C(═O)R¹⁰, CONR¹⁰ R¹¹, OC(═O)R¹⁰, OC(═O)OR²¹, OR¹⁰, OC(═O)NR¹⁰ R¹¹, OCH₂ CO₂ R¹⁰, CO₂ CH₂ CO₂ R¹⁰, NO₂, NR¹⁰ C(═O)R¹⁰, NR¹⁰ C(═O)OR²¹, NR¹⁰ C(═O)NR¹⁰ R¹¹, NR¹⁰ SO₂ NR¹⁰ R¹¹, NR¹⁰ SO₂ R²¹, S(O)_(p) R¹¹, SO₂ NR¹⁰ R¹¹, SiMe₃, C₂ to C₆ alkenyl, C₃ to C₁₁ cycloalkyl, C₄ to C₁₁ cycloalkylmethyl, C₆ to C₁₀ aryl, or C₇ to C₁₁ arylalkyl; R⁸ is selected from:H, R⁶, C₁ -C₁₀ alkyl, substituted with 0-3 R⁶, C₂ -C₁₀ alkenyl, substituted with 0-3 R⁶, C₂ -C₁₀ alkynyl, substituted with 0-3 R⁶, C₃ -C₈ cycloalkyl, substituted with 0-3 R⁶, C₅ -C₆ cycloalkenyl, substituted with 0-3 R⁶, aryl, substituted with 0-3 R⁶, or - 10membered heterocyclic ring containing 1-3 N, O, or S heteroatoms, wherein said heterocyclic ring is saturated, partially saturated, or fully unsaturated, said heterocyclic ring being substituted with 0-2 R⁷ ; R⁹ is selected from H, hydroxy, C₁ -C₁₀ alkoxy, nitro, N(R¹⁰)R¹¹, --N(R¹⁶)R¹⁷, OR²², C₁ -C₁₀ alkyl substituted with 0-3 R⁷, aryl substituted with 0-3 R⁷, heteroaryl substituted with 0-3 R⁷, C₁ -C₁₀ alkylcarbonyl; aryl(C₀ -C₆ alkyl)carbonyl, C₁ -C₁₀ alkenyl, C₁ -C₁₀ alkynyl, C₃ -C₁₀ cycloalkyl, C₃ -C₁₀ cycloalkylalkyl, aryl(C₁ -C₆ alkyl)-, heteroaryl(C₁ -C₆ alkyl)-, CO₂ R^(18a), C(═O)R^(18a), CONR^(18a) R²⁰, SO₂ R^(18a), or SO₂ NR^(18a) R²⁰, provided that any of the above alkyl, cycloalkyl, aryl or heteroaryl groups are unsubstituted or substituted independently with 0-2 R⁷ ; R¹⁰ is selected from H, C₁ -C₈ alkyl, C₃ -C₆ alkenyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylmethyl, C₆ -C₁₀ aryl, C₇ -C₁₁ arylalkyl, or C₁ -C₁₀ alkyl substituted with 0-2 R⁴ ; R¹¹ is selected from hydrogen, hydroxy, C₁ to C₈ alkyl, C₃ -C₆ alkenyl, C₃ to C₁₁ cycloalkyl, C₄ to C₁₁ cycloalkylmethyl, C₁ -C₆ alkoxy, benzyloxy, C₆ to C₁₀ aryl, heteroaryl, heteroarylalkyl, C₇ to C₁₁ arylalkyl, adamantylmethyl, or C₁ -C₁₀ alkyl substituted with 0-2 R⁴ ; alternatively, R¹⁰ and R¹¹ when both are substituents on the same nitrogen atom are taken together with the nitrogen atom to which they are attached to form a heterocycle selected from: 3-azabicyclononyl, 1,2,3,4-tetrahydro-1-quinolinyl, 1,2,3,4-tetrahydro-2-isoquinolinyl, 1-piperidinyl, 1-morpholinyl, 1-pyrrolidinyl, thiamorpholinyl, thiazolidinyl or 1-piperazinyl; said heterocycle being optionally substituted with 0-3 groups selected from: C₁ -C₆ alkyl, C₆ -C₁₀ aryl, heteroaryl, C₇ -C₁₁ arylalkyl, C₁ -C₆ alkylcarbonyl, C₃ -C₇ cycloalkylcarbonyl, C₁ -C₆ alkoxycarbonyl, C₇ -C₁₁ arylalkoxycarbonyl, C₁ -C₆ alkylsulfonyl or C₆ -C₁₀ arylsulfonyl; R¹² is selected from:H, C₁ -C₁₀ alkyl, triphenylmethyl, methoxyphenyldiphenylmethyl, trimethylsilylethoxymethyoxy, C₁ -C₁₀ alkoxycarbonyl, C₁ -C₁₀ alkylcarbonyl, C₁ -C₁₀ alkylsulfonyl, aryl(C₁ -C₁₀ alkyl)sulfonyl, arylsulfonyl, aryl(C₂ -C₁₀ alkenyl)sulfonyl, heteroarylsulfonyl, aryl, C₂ -C₆ alkenyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, C₇ -C₁₁ arylalkyl, C₇ -C₁₁ arylcarbonyl, C₄ -C₁₁ cycloalkoxycarbonyl, C₇ -C₁₁ bicycloalkoxycarbonyl, C₇ -C₁₁ aryloxycarbonyl, heteroarylcarbonyl, heteroarylalkylcarbonyl, or aryl(C₁ -C₁₀ alkoxy)carbonyl; wherein said aryl groups are optionally substituted with 0-3 substituents selected from the group consisting of: C₁ -C₄ alkyl, C₁ -C₄ alkoxy, halo, CF₃, and NO₂ ; R¹³ is selected from: H, hydroxy, C₁ -C₁₀ alkoxy, nitro, N(R¹⁰)R¹¹, --N(R¹⁶)R¹⁷, C₁ -C₁₀ alkyl substituted with 0-3 R⁷, aryl substituted with 0-3 R⁷, heteroaryl substituted with 0-3 R⁷, or C₁ -C₁₀ alkylcarbonyl; R¹⁴ is selected from H, C₁ -C₁₀ alkyl, C₂ -C₁₀ alkenyl, C₂ -C₁₀ alkynyl, C₁ -C₁₀ alkoxy, aryl, heteroaryl or C₁ -C₁₀ alkoxycarbonyl, CO₂ R¹⁰ or --C(═O)N(R¹⁰)R¹¹ ; R¹⁵ is selected from:H, R⁶, --CO₂ R¹⁰, --C(═O)N(R¹⁰)R¹¹ ; C₁ -C₁₀ alkoxycarbonyl substituted with 0-2 R⁶ ; C₁ -C₁₀ alkyl, substituted with 0-3 R⁶ ; C₂ -C₁₀ alkenyl, substituted with 0-3 R⁶ ; C₁ -C₁₀ alkoxy, substituted with 0-3 R⁶ ; aryl, substituted with 0-3 R⁶ ; or 5-10 membered heterocyclic ring containing 1-3 N, O, or S heteroatoms, wherein said heterocyclic ring is saturated, partially saturated, or fully unsaturated, said heterocyclic ring being substituted with 0-2 R⁷ ; R¹⁶ is selected from:--C(═O)--O--R^(18a), --C(═O)--R^(18b), --C(═O)N(R^(18b))₂, --C(═O)NHSO₂ R^(18a), --C(═O)NHC(═O)R^(18b), --C(═O)NHC(═O)OR^(18a), --C(═O)NHSO₂ NHR^(18b), --C(═S)--NH--R^(18b), --NH--C(═O)--O--R^(18a), --NH--C(═O)--R^(18b), --NH--C(═O)--NH--R^(18b), --SO₂ --O--R^(18a), --SO₂ --R^(18a), --SO₂ --N(R^(18b))₂, --SO₂ --NHC(═O)OR^(18b) ; R¹⁷ is selected from: H, C₁ -C₁₀ alkyl, C₂ -C₆ alkenyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₅ cycloalkylalkyl, aryl, aryl(C₁ -C₁₀ alkyl)-; R^(18a) is selected from:C₁ -C₈ alkyl substituted with 0-2 R¹⁹, C₂ -C₈ alkenyl substituted with 0-2 R¹⁹, C₂ -C₈ alkynyl substituted with 0-2 R¹⁹, C₃ -C₈ cycloalkyl substituted with 0-2 R¹⁹, aryl substituted with 0-4 R¹⁹, aryl(C₁ -C₆ alkyl)- substituted with 0-4 R¹⁹, a 5-10 membered heterocyclic ring system having 1-3 heteroatoms selected independently from O, S, and N, said heterocyclic ring being substituted with 0-4 R¹⁹, C₁ -C₆ alkyl substituted with a 5-10 membered heterocyclic ring system having 1-3 heteroatoms selected independently from O, S, and N, said heterocyclic ring being substituted with 0-4 R¹⁹ ; R^(18b) is selected from R^(18a) or H; R¹⁹ is selected from H, halogen, CF₃, CO₂ H, CN, NO₂, NR¹¹ R¹², C₁ -C₈ alkyl, C₂ -C₆ alkenyl, C₂ -C₆ alkynyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, aryl(C₁ -C₆ alkyl)-, C₁ -C₆ alkoxy, OCF₃, or C₁ -C₄ alkoxycarbonyl, aryl, --O-aryl, --SO₂ -aryl, heteroaryl, or --SO₂ -heteroaryl, wherein said aryl and heteroaryl groups are substituted with 0-4 groups selected from hydrogen, halogen, CF₃, C₁ -C₃ alkyl, or C₁ -C₃ alkoxy; R²⁰ is selected from hydroxy, C₁ to C₁₀ alkyloxy, C₃ to C₁₁ cycloalkyloxy, C₆ to C₁₀ aryloxy, C₇ to C₁₁ arylalkyloxy, C₃ to C₁₀ alkylcarbonyloxyalkyloxy, C₃ to C₁₀ alkoxycarbonyloxyalkyloxy, C₂ to C₁₀ alkoxycarbonylalkyloxy, C₅ to C₁₀ cycloalkylcarbonylomyalkyloxy, C₅ to C₁₀ cycloalkoxycarbonyloxyalkyloxy, C₅ to C₁₀ cycloalkoxycarbonylalkyloxy, C₇ to C₁₁ aryloxycarbonylalkyloxy, C₈ to C₁₂ aryloxycarbonyloxyalkyloxy, C₈ to C₁₂ arylcarbonyloxyalkyloxy, C₅ to C₁₀ alkoxyalkylcarbonyloxyalkyloxy, C₅ to C₁₀ (5-alkyl-1,3-dioxa-cyclopenten-2-one-yl)methyloxy, C₁₀ to C₁₄ (5-aryl-1,3-dioxa-cyclopenten-2-one-yl)methyloxy, (R¹¹)(R¹²)N--(C₁ -C₁₀ alkoxy)-; R²¹ is selected from: C₁ -C₈ alkyl, C₂ -C₆ alkenyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylmethyl, C₆ -C₁₀ aryl, C₇ -C₁₁ arylalkyl, or C₁ -C₁₀ alkyl substituted with 0-2 R⁵ ; R²² is selected from:--C(═O)--R^(18b), --C(═O)N(R^(18b))₂, --C(═O)NHSO₂ R^(18a), --C(═O)NHC(═O)R^(18b), --C(═O)NHC(═O)OR^(18a), --C(═O)NHSO₂ NHR^(18b), --C(═S)--NH--R^(18b), --SO₂ --R^(18a), --SO₂ --N(R^(18b))₂, --SO₂ --NHC(═O)OR^(18b) ; m is 0-2; n is 0-4; p is 0-2; q is 0-4; r is 0-2; s is 0-1; with the following provisos:(1) when b is a double bond, only one of R¹⁴ or R¹⁵ is present and Q and U are not --(CH₂)--; and (2) n, m and q are chosen such that the number of atoms connecting R¹ and Y is in the range of 8-14; and (3) when V is -(phenyl)-Q--, then either: U is not a direct bond or Q is not a direct bond.
 2. A compound of claim 1 of Formula I: ##STR43## including stereoisomeric forms thereof, or mixtures of stereoisomeric forms thereof, or a pharmaceutically acceptable salt thereof wherein:b, the bond between carbon atoms numbered 4 and 5, is a carbon-carbon single or double bond; R¹ is selected from: ##STR44## A is selected from --CH₂ --, or --N(R¹²)--; A¹ and B are independently --CH₂ -- or --N(R¹⁰)--; D is --N(R¹²)--, or --S--; E--F is --C(R²)═C(R³)--, or --C(R²)₂ C(R³)₂ --; J is either --C(R²)-- or --N--, and K, L and M are independently selected from --C(R²)-- or --C(R³)--; R² and R³ are independently selected from: H, C₁ -C₄ alkoxy, NR¹¹ R¹², ═NR¹², halogen, NO₂, CN, CF₃, C₁ -C₆ alkyl, C₃ -C₆ alkenyl, C₃ -C₇ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, C₆ -C₁₀ aryl substituted with 0-4 R⁷, C₇ -C₁₁ arylalkyl, C₂ -C₇ alkylcarbonyl, C₁ -C₄ alkoxycarbonyl, or C₇ -C₁₁ arylcarbonyl; alternatively, R² and R³ when substituents on adjacent atoms, are taken together when substituents on adjacent atoms, with the carbon atoms to which they are attached, to form a 5-7 membered carbocyclic or 5-7 membered heterocyclic with the carbon atoms to which they are attached, aromatic or nonaromatic ring system, said carbocyclic or heterocyclic ring being optionally substituted with 0-2 groups selected from C₁ -C₄ alkyl, C₁ -C₄ alkoxy, halo, cyano, amino, CF₃ or NO₂ ; R^(2a) is absent or R¹² ; U is selected from:--(CH₂)_(n) --, --(CH₂)_(n) O(CH₂)_(m) --, --(CH₂)_(n) N(R¹²)(CH₂)_(m) --, --(CH₂)_(n) C(═O)(CH₂)_(m) --, --(CH₂)_(n) S(O)_(p) (CH₂)_(m) --, --(CH₂)_(n) NHNH(CH₂)_(m) --, --N(R¹⁰)C(═O)--, or --C(═O)N(R¹⁰)--; --N(R¹⁰)S(O)_(p) --, or V is selected from:--(CH₂)_(n) --, --(C₁ -C₆ alkylene)-Q--, substituted with 0-3 groups independently selected from R¹³, --(C₂ -C₇ alkenylene)-Q--, substituted with 0-3 groups independently selected from R¹³, --(C₂ -C₇ alkynylene)-Q--, substituted with 0-3 groups independently selected from R¹³, -(phenyl)-Q--, said phenyl substituted with 0-2 groups independently selected from R¹³, -(pyridyl)-Q--, said pyridyl substituted with 0-2 groups independently selected from R¹³, or -(pyridazinyl)-Q--, said pyridazinyl substituted with 0-2 groups independently selected from R¹³ ; Q is selected from:--(CH₂)_(n) --, --(CH₂)_(n) O(CH₂)_(m) --, --(CH₂)_(n) N(R¹²)(CH₂)_(m) --, --(CH₂)_(n) C(═O)(CH₂)_(m) --, --(CH₂)_(n) S(O)_(p) (CH₂)_(m) --, --(CH₂)_(n) NHNH(CH₂)_(m) --, --N(R¹⁰)C(═O)--, or --C(═O)N(R¹⁰)--; W is selected from:--(C(R⁴)₂)_(q) C(═O)N(R¹⁰)-- or, --C(═O)--N(R¹⁰)--(C(R⁴)₂)_(q) --; X is selected from:a single bond or, --(C(R⁴)₂)_(q) -- C(R⁴)(R⁸)!_(s) --C(R⁴)(R⁹)--; alternatively, W is ##STR45## and X is either absent or --CH₂ --Y is selected from:--COR²⁰, --SO₃ H, --PO₃ H, --CONHNHSO₂ CF₃, --CONHSO₂ R^(18a), --CONHSO₂ NHR^(18b), --NHCOCF₃, --NHCONHSO₂ R^(18a), --NHSO₂ R^(18a), --OPO₃ H₂, --OSO₃ H, --PO₃ H₂, --SO₃ H, --SO₂ NHCOR^(18a), --SO₂ NHCO₂ R^(18a), or ##STR46## Z is selected from --CH(R⁹)--, or --N(R¹⁶)--; R⁴ is selected from H, C₁ -C₁₀ alkyl, C₁ -C₁₀ alkylcarbonyl, aryl, arylalkyl, cycloalkyl, or cycloalkylalkyl; alternatively, two R⁴ groups on adjacent carbon atoms join to form a bond, thereby forming a carbon-carbon double or triple bond between the adjacent carbon atoms; R⁶ is selected from:H, C₁ -C₁₀ alkyl, hydroxy, C₁ -C₁₀ alkoxy, nitro, C₁ -C₁₀ alkylcarbonyl, --N(R¹¹)R¹², cyano, halo, CF₃, CHO, CO₂ R^(18b), C(═O)R^(18b), CONR¹⁷ R^(18b), OC(═O)R¹⁰, OR¹⁰, OC(═O)NR¹⁰ R¹¹, NR¹⁰ C(═O)R¹⁰, NR¹⁰ C(═O)OR²¹, NR¹⁰ C(═O)NR¹⁰ R¹¹, NR¹⁰ SO₂ NR¹⁰ R¹¹, NR¹⁰ SO₂ R²¹, S(O)_(p) R¹¹, SO₂ NR¹⁰ R¹¹, C₆ to C₁₀ aryl optionally substituted with 0-3 groups selected from halogen, C₁ -C₆ alkoxy, C₁ -C₆ alkyl, CF₃, S(O)_(m) Me, or --NMe₂ ; C₇ to C₁₁ arylalkyl, said aryl being optionally substituted with 1-3 groups selected from halogen, C₁ -C₆ alkoxy, C₁ -C₆ alkyl, CF₃, S(O)_(p) Me, or --NMe₂, a 5-10 membered heterocyclic ring containing 1-3 N, O, or S heteroatoms, wherein said heterocyclic ring is saturated, partially saturated, or fully unsaturated, said heterocyclic ring being substituted with 0-2 R⁷ ; R⁷ is selected from selected from H, C₁ -C₄ alkyl, hydroxy, C₁ -C₄ alkoxy, C₆ -C₁₀ aryl, C₇ -C₁₁ arylalkyl, (C₁ -C₄ alkyl)carbonyl, CO₂ R^(18a), SO₂ R¹¹, SO₂ NR¹⁰ R¹¹, OR¹⁰, or N(R¹¹)R¹² ; R⁸ is selected from:H, CO₂ R^(18a), C(═O)R^(18a), or CONR¹⁷ R^(18a) C₁ -C₁₀ alkyl, substituted with 0-1 R⁶, C₂ -C₁₀ alkenyl, substituted with 0-1 R⁶, C₂ -C₁₀ alkynyl, substituted with 0-1 R⁶, C₃ -C₈ cycloalkyl, substituted with 0-1 R⁶, C₅ -C₆ cycloalkenyl, substituted with 0-1 R⁶, aryl, substituted with 0-3 R⁶, or - 10membered heterocyclic ring containing 1-3 N, O, or S heteroatoms, wherein said heterocyclic ring is saturated, partially saturated, or fully unsaturated, said heterocyclic ring being substituted with 0-2 R⁷ ; R⁹ is selected from H, hydroxy, C₁ -C₁₀ alkoxy, nitro, N(R¹⁰)R¹¹, --N(R¹⁶)R¹⁷, OR²², C₁ -C₁₀ alkyl substituted with 0-3 R⁷, aryl substituted with 0-3 R⁷, heteroaryl substituted with 0-3 R⁷, C₁ -C₁₀ alkylcarbonyl; aryl(C₀ -C₆ alkyl)carbonyl, C₁ -C₁₀ alkenyl, C₁ -C₁₀ alkynyl, C₃ -C₁₀ cycloalkyl, C₃ -C₁₀ cycloalkylalkyl, aryl(C₁ -C₆ alkyl)-, heteroaryl(C₁ -C₆ alkyl)-, CO₂ R^(18a), C(═O)R^(18a), CONR^(18a) R²⁰, SO₂ R^(18a), or SO₂ NR^(18a) R²⁰, provided that any of the above alkyl, cycloalkyl, aryl or heteroaryl groups are unsubstituted or substituted independently with 0-2 R⁷ ; R¹⁰ is selected from H, C₁ -C₈ alkyl, C₃ -C₆ alkenyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylmethyl, C₆ -C₁₀ aryl, C₇ -C₁₁ arylalkyl, or C₁ -C₁₀ alkyl substituted with 0-2 R⁴ ; R¹¹ is selected from hydrogen, hydroxy, C₁ to C₈ alkyl, C₃ -C₆ alkenyl, C₃ to C₁₁ cycloalkyl, C₄ to C₁₁ cycloalkylmethyl, C₁ -C₆ alkoxy, benzyloxy, C₆ to C₁₀ aryl, heteroaryl, heteroarylalkyl, C₇ to C₁₁ arylalkyl, adamantylmethyl, or C₁ -C₁₀ alkyl substituted with 0-2 R⁴ ; alternatively, R¹⁰ and R¹¹ when both are substituents on the same nitrogen atom are taken together with the nitrogen atom to which they are attached to form a heterocycle selected from: 3-azabicyclononyl, 1,2,3,4-tetrahydro-1-quinolinyl, 1,2,3,4-tetrahydro-2-isoquinolinyl, 1-piperidinyl, 1-morpholinyl, 1-pyrrolidinyl, thiamorpholinyl, thiazolidinyl or 1-piperazinyl; said heterocycle being optionally substituted with 0-3 groups selected from: C₁ -C₆ alkyl, C₆ -C₁₀ aryl, heteroaryl, C₇ -C₁₁ arylalkyl, C₁ -C₆ alkylcarbonyl, C₃ -C₇ cycloalkylcarbonyl, C₁ -C₆ alkoxycarbonyl, C₇ -C₁₁ arylalkoxycarbonyl, C₁ -C₆ alkylsulfonyl or C₆ -C₁₀ arylsulfonyl; R¹² is selected from:H, C₁ -C₆ alkyl, triphenylmethyl, methoxyphenyldiphenylmethyl, trimethylsilylethoxymethyoxy, (C₁ -C₆ alkyl)carbonyl, (C₁ -C₆ alkoxy)carbonyl; (C₁ -C₆ alkyl)aminocarbonyl, C₃ -C₆ alkenyl, C₃ -C₇ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, aryl, heteroaryl(C₁ -C₆ alkyl)carbonyl, heteroarylcarbonyl, aryl C₁ -C₆ alkyl, (C₁ -C₆ alkyl)carbonyl, or arylcarbonyl, C₁ -C₆ alkylsulfonyl, arylsulfonyl, aryl(C₁ -C₆ alkyl)sulfonyl, heteroarylsulfonyl, heteroaryl(C₁ -C₆ alkyl)sulfonyl, aryloxycarbonyl, or aryl(C₁ -C₆ alkoxy)carbonyl, wherein said aryl groups are substituted with 0-2 substituents selected from the group consisting of C₁ -C₄ alkyl, C₁ -C₄ alkoxy, halo, CF₃, and nitro; R¹³ is selected from: H, hydroxy, C₁ -C₁₀ alkoxy, nitro, N(R¹⁰)R¹¹, --N(R¹⁶)R¹⁷, C₁ -C₁₀ alkyl substituted with 0-3 R⁷, aryl substituted with 0-3 R⁷, heteroaryl substituted with 0-3 R⁷, or C₁ -C₁₀ alkylcarbonyl; R¹⁴ is selected from H, C₁ -C₁₀ alkyl, C₂ -C₁₀ alkenyl, C₂ -C₁₀ alkynyl, C₁ -C₁₀ alkoxy, aryl, heteroaryl or C₁ -C₁₀ alkoxycarbonyl, CO₂ R¹⁰ or --C(═O)N(R¹⁰)R¹¹ ; R¹⁵ is selected from: H, CO₂ R^(18a), C(═O)R^(18a), CONR^(18a) R¹⁷, --SO₂ R^(18a), --SO₂ NR^(18a) R¹⁷, C₁ -C₆ alkyl substituted with 0-1 R⁹, C₃ -C₆ alkenyl substituted with 0-1 R⁹, C₃ -C₇ cycloalkyl substituted with 0-1 R⁹, C₄ -C₁₁ cycloalkylalkyl substituted with 0-1 R⁹, aryl substituted with 0-1 R⁹ or 0-2 R⁷, or aryl(C₁ -C₆ alkyl)- substituted with 0-1 R⁹ or 0-2 R⁷ ; R¹⁶ is selected from:--C(═O)--O--R^(18a), --C(═O)--R^(18b), --C(═O)N(R^(18b))₂, --C(═O)NHSO₂ R^(18a), --C(═O)NHC(═O)R^(18b), --C(═O)NHC(═O)OR^(18a), --C(═O)NHSO₂ NHR^(18b), --SO₂ --R^(18a), --SO₂ --N(R^(18b))₂ or, --SO₂ --NHC(═O)OR^(18b) ; R¹⁷ is selected from: H, C₁ -C₆ alkyl, C₃ -C₇ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, aryl, aryl(C₁ -C₆ alkyl)-, or heteroaryl (C₁ -C₆ alkyl); R^(18a) is selected from: C₁ -C₈ alkyl, C₃ -C₁₁ cycloalkyl, aryl(C₁ -C₆ alkyl)-, (C₁ -C₆ alkyl)aryl, heteroaryl(C₁ -C₆ alkyl)-, (C₁ -C₆ alkyl)heteroaryl, biaryl(C₁ -C₆ alkyl), heteroaryl, or aryl, wherein said aryl or heteroaryl groups are optionally substituted with 0-4 R¹⁹ ; R^(18b) is selected from R^(18a) or H; R¹⁹ is selected from H, halogen, CF₃, CO₂ H, CN, NO₂, NR¹¹ R¹², C₁ -C₈ alkyl, C₂ -C₆ alkenyl, C₂ -C₆ alkynyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, aryl(C₁ -C₆ alkyl)-, C₁ -C₆ alkoxy, OCF₃, or C₁ -C₄ alkoxycarbonyl, aryl, --O-aryl, --SO₂ -aryl, heteroaryl, or --SO₂ -heteroaryl, wherein said aryl and heteroaryl groups are substituted with 0-4 groups selected from hydrogen, halogen, CF₃, C₁ -C₃ alkyl, or C₁ -C₃ alkoxy; R²⁰ is selected from hydroxy, C₁ to C₁₀ alkyloxy, C₃ to C₁₁ cycloalkyloxy, C₆ to C₁₀ aryloxy, C₇ to C₁₁ aralkyloxy, C₃ to C₁₀ alkylcarbonyloxyalkyloxy, C₃ to C₁₀ alkoxycarbonyloxyalkyloxy, C₂ to C₁₀ alkoxycarbonylalkyloxy, C₅ to C₁₀ cycloalkylcarbonyloxyalkyloxy, C₅ to C₁₀ cycloalkoxycarbonyloxyalkyloxy, C₅ to C₁₀ cycloalkoxycarbonylalkyloxy, C₇ to C₁₁ aryloxycarbonylalkyloxy, C₈ to C₁₂ aryloxycarbonyloxyalkyloxy, C₈ to C₁₂ arylcarbonyloxyalkyloxy, C₅ to C₁₀ alkoxyalkylcarbonyloxyalkyloxy, C₅ to C₁₀ (5-alkyl-1,3-dioxa-cyclopenten-2-one-yl)methyloxy, C₁₀ to C₁₄ (5-aryl-1,3-dioxa-cyclopenten-2-one-yl)methyloxy, or (R¹¹)(R¹²)N--(C₁ -C₁₀ alkoxy)-; R²¹ is selected from: C₁ -C₈ alkyl, C₂ -C₆ alkenyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylmethyl, C₆ -C₁₀ aryl, C₇ -C₁₁ arylalkyl, or C₁ -C₁₀ alkyl substituted with 0-2 R⁷ ; R²² is selected from:--C(═O)--R^(18b), --C(═O)N(R^(18b))₂, --C(═O)NHSO₂ R^(18a), --C(═O)NHC(═O)R^(18b), --C(═O)NHC(═O)OR^(18a) or, --C(═O)NHSO₂ NHR^(18b), m is 0-2; n is 0-4; p is 0-2; q is 0-4; r is 0-2; s is 0-1; with the following provisos:(1) when b is a double bond, only one of R¹⁴ or R¹⁵ is present and Q and U are not --(CH₂)--; and (2) n, m and q are chosen such that the number of atoms connecting R¹ and Y is in the range of 8--14; and (3) when V is -(phenyl)-Q--, then either: U is not a direct bond (i.e., U is not --(CH₂)_(n) -- where n=0) or Q is not a direct bond (i.e., Q is not --(CH₂)_(n) -- where n=0).
 3. A compound of claim 2 of Formula II: ##STR47## including enantiomeric or diastereomeric forms thereof, or mixtures of enantiomeric or diastereomeric forms thereof, or a pharmaceutically acceptable salt thereof wherein:b, the bond between carbon atoms numbered 4 and 5, is a carbon-carbon single or double bond; R¹ is selected from: ##STR48## R² and R³ are independently selected from: H, C₁ -C₄ alkoxy, NR¹¹ R¹², halogen, NO₂, CN, CF₃, C₁ -C₆ alkyl, C₃ -C₆ alkenyl, C₃ -C₇ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, C₆ -C₁₀ aryl substituted with 0-2 R⁷, C₇ -C₁₁ arylalkyl, C₂ -C₇ alkylcarbonyl, or C₇ -C₁₁ arylcarbonyl;alternatively, R² and R³ are taken together with the carbon atoms to which they are attached to form a 5-7 membered carbocyclic or 5-7 membered heterocyclic aromatic or nonaromatic ring system, said carbocyclic or heterocyclic ring being optionally substituted with 0-2 R⁷ ; U is selected from:--(CH₂)_(n) --, --N(R¹²)(CH₂)_(m) --, --N(R¹⁰)C(═O)--, or --C(═O)N(R¹⁰)--; --N(R¹⁰)S(O)_(p) --, or V is selected from:--(CH₂)_(n) --, --(C₁ -C₆ alkylene)-Q--, substituted with 0-3 groups independently selected from R¹³, --(C₂ -C₇ alkenylene)-Q--, substituted with 0-3 groups independently selected from R¹³, --(C₂ -C₇ alkynylene)-Q--, substituted with 0-3 groups independently selected from R¹³, -(phenyl)-Q--, said phenyl substituted with 0-2 groups independently selected from R¹³, -(pyridyl)-Q--, said pyridyl substituted with 0-2 groups independently selected from R¹³, or -(pyridazinyl)-Q--, said pyridazinyl substituted with 0-2 groups independently selected from R¹³ ; Q is selected from:--(CH₂)_(n) --, --(CH₂)_(n) O(CH₂)_(m) --, --(CH₂)_(n) N(R¹²)(CH₂)_(m) --, --N(R¹⁰)C(═O)--, or --C(═O)N(R¹⁰)--; W is selected from:--(CH₂)_(q) C(═O)N(R¹⁰)--, or --C(═O)--N(R¹⁰)--(CH₂)_(q) --; X is --(CH₂)_(q) --CH(R⁸)--CH(R⁹)--; Y is --COR²⁰ ; R⁶ is selected from:H, C₁ -C₄ alkyl, hydroxy, C₁ -C₄ alkoxy, nitro, C₁ -C₆ alkylcarbonyl, --N(R¹¹)R¹², cyano, halo, CF₃, --S(O)_(p) R¹⁰, CO₂ R^(18a), CONR¹⁷ R^(18a), --COR^(18a), OR¹⁰, C₆ to C₁₀ aryl optionally substituted with 0-3 groups selected from halogen, C₁ -C₆ alkoxy, C₁ -C₆ alkyl, CF₃, S(O)_(m) Me, or --NMe₂ ; a heterocyclic ring system selected from pyridinyl, furanyl, thiazolyl, thienyl, pyrrolyl, pyrazolyl, triazolyl, imidazolyl, benzofuranyl, indolyl, indolinyl, quinolinyl, isoquinolinyl, benzimidazolyl, piperidinyl, tetrahydrofuranyl, pyranyl, 3H-indolyl, carbazolyl, pyrrolidinyl, piperidinyl, isoxazolinyl, isoxazolyl, or morpholinyl; R⁷ is selected from:H, C₁ -C₄ alkyl, hydroxy, C₁ -C₄ alkoxy, nitro, C₁ -C₄ alkylcarbonyl, --N(R¹¹)R¹², CO₂ R^(18a), SO₂ R¹¹, SO₂ NR¹⁰ R¹¹ or OR¹⁰ ; R⁸ is selected from:H, CONR¹⁷ R^(18a), --CO₂ R^(18a), --COR^(18a) C₁ -C₁₀ alkyl, substituted with 0-1 R⁶, C₂ -C₁₀ alkenyl, substituted with 0-1 R⁶, C₂ -C₁₀ alkynyl, substituted with 0-1 R⁶, C₃ -C₈ cycloalkyl, substituted with 0-1 R⁶, aryl, substituted with 0-1 R⁶ or, a heterocyclic ring system selected from pyridinyl, furanyl, thiazolyl, thienyl, pyrrolyl, pyrazolyl, triazolyl, imidazolyl, benzofuranyl, indolyl, indolinyl, quinolinyl, isoquinolinyl, benzimidazolyl, piperidinyl, tetrahydrofuranyl, pyranyl, 3H-indolyl, carbazolyl, pyrrolidinyl, piperidinyl, isoxazolinyl, isoxazolyl or morpholinyl, said heterocycle optionally substituted with 0-2 R⁷ ; R⁹ is selected from: H or --N(R¹⁶)R¹⁷ ; R¹⁰ is selected from H or C₁ -C₁₀ alkyl, or C₇ -C₁₀ arylalkyl; R¹¹ is selected from hydrogen, hydroxy, C₁ to C₈ alkyl, C₃ -C₆ alkenyl, C₃ to C₁₁ cycloalkyl, C₄ to C₁₁ cycloalkylmethyl, C₁ -C₆ alkoxy, benzyloxy, C₆ to C₁₀ aryl, heteroaryl, heteroarylalkyl, C₇ to C₁₁ arylalkyl, adamantylmethyl, or C₁ -C₁₀ alkyl substituted with 0-2 R⁴ ; alternatively, R¹⁰ and R¹¹ when both are substituents on the same nitrogen atom are taken together with the nitrogen atom to which they are attached to form a heterocycle selected from: 3-azabicyclononyl, 1,2,3,4-tetrahydro-1-quinolinyl, 1,2,3,4-tetrahydro-2-isoquinolinyl, 1-piperidinyl, 1-morpholinyl, 1-pyrrolidinyl, thiamorpholinyl, thiazolidinyl or 1-piperazinyl; said heterocycle being optionally substituted with 1-3 groups selected from: C₁ -C₆ alkyl, C₆ -C₁₀ aryl, heteroaryl, C₇ -C₁₁ arylalkyl, C₁ -C₆ alkylcarbonyl, C₃ -C₇ cycloalkylcarbonyl, C₁ -C₆ alkoxycarbonyl, C₇ -C₁₁ arylalkoxycarbonyl, C₁ -C₆ alkylsulfonyl or C₆ -C₁₀ arylsulfonyl; R¹² is selected from:H, C₁ -C₆ alkyl, triphenylmethyl, methoxyphenyldiphenylmethyl, trimethylsilylethoxymethyoxy, C₁ -C₄ alkoxycarbonyl, C₁ -C₆ alkylcarbonyl, C₁ -C₆ alkylsulfonyl, aryl(C₁ -C₄ alkyl)sulfonyl, arylsulfonyl, aryl, heteroarylcarbonyl, or heteroarylalkylcarbonyl, wherein said aryl groups are substituted with 0-3 substituents selected from the group consisting of: C₁ -C₄ alkyl, C₁ -C₄ alkoxy, halo, CF₃, and NO₂ ; R¹³ is selected from: H, hydroxy, C₁ -C₁₀ alkoxy, N(R¹⁰)R¹¹, --N(R¹⁶)R¹⁷, C₁ -C₁₀ alkyl substituted with 0-3 R⁷, aryl substituted with 0-3 R⁷, heteroaryl substituted with 0-3 R⁷, or C₁ -C₁₀ alkylcarbonyl; R¹⁴ is selected from H, C₁ -C₁₀ alkyl, C₂ -C₁₀ alkenyl, C₂ -C₁₀ alkynyl, C₁ -C₁₀ alkoxy, aryl, heteroaryl or C₁ -C₁₀ alkoxycarbonyl, CO₂ R¹⁰ or --C(═O)N(R¹⁰)R¹¹ ; R¹⁶ is selected from:--C(═O)--O--R^(18a), --C(═O)--R^(18b), --SO₂ --R^(18a) or, --SO₂ --N(18^(b))₂ ; R¹⁷ is selected from H or C₁ -C₄ alkyl; R^(18a) is selected from: C₁ -C₈ alkyl, C₃ -C₁₁ cycloalkyl, aryl(C₁ -C₆ alkyl)-, (C₁ -C₆ alkyl)aryl, heteroaryl(C₁ -C₆ alkyl)-, (C₁ -C₆ alkyl)heteroaryl, biaryl(C₁ -C₆ alkyl), heteroaryl, or aryl, wherein said aryl or heteroaryl groups are optionally substituted with 0-2 R¹⁹ ; R^(18b) is selected from R^(18a) or H; R¹⁹ is selected from H, halogen, CF₃, CO₂ H, CN, NO₂, NR¹¹ R¹², C₁ -C₈ alkyl, C₂ -C₆ alkenyl, C₂ -C₆ alkynyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylalkyl, aryl(C₁ -C₆ alkyl)-, C₁ -C₆ alkoxy, OCF₃, or C₁ -C₄ alkoxycarbonyl, aryl, --O-aryl, --SO₂ -aryl, heteroaryl, or --SO₂ -heteroaryl, wherein said aryl and heteroaryl groups are substituted with 0-4 groups selected from hydrogen, halogen, CF₃, C₁ -C₃ alkyl, or C₁ -C₃ alkoxy; R²⁰ is selected from:hydroxy; C₁ to C₁₀ alkoxy; methylcarbonyloxymethoxy-; ethylcarbonyloxymethoxy-; t-butyl carbonyloxymethoxy-; cyclohexylcarbonyloxymethoxy-; 1-(methylcarbonyloxy)ethoxy-; 1-(ethylcarbonyloxy)ethoxy-; 1-(t-butylcarbonyloxy)ethoxy-; 1-(cyclohexylcarbonyloxy)ethoxy-; i-propyloxycarbonyloxymethoxy-; t-butyloxycarbonyloxymethoxy-; 1-(i-propyloxycarbonyloxy)ethoxy-; 1-(cyclohexyloxycarbonyloxy)ethoxy-; 1-(t-butyloxycarbonyloxy)ethoxy-; dimethylaminoethoxy-; diethylaminoethoxy-; (5-methyl-1,3-dioxacyclopenten-2-on-4-yl)methoxy-; (5-(t-butyl)-1,3-dioxacyclopenten-2-on-4-yl)methoxy-; (1,3-dioxa-5-phenyl-cyclopenten-2-on-4-yl)methoxy- or; 1-(2-(2-methoxypropyl)carbonyloxy)ethoxy-; R²¹ is selected from C₁ -C₈ alkyl, C₂ -C₆ alkenyl, C₃ -C₁₁ cycloalkyl, C₄ -C₁₁ cycloalkylmethyl, C₆ -C₁₀ aryl, C₇ -C₁₁ arylalkyl, or C₁ -C₁₀ alkyl substituted with 0-2 R⁴ ; m is 0-2; n is 0-4; p is 0-2; q is 0-1; and r is 0-2; with the following provisos:(1) when b is a double bond, Q and U are not --(CH₂)--; and (2) n, m and q are chosen such that the number of atoms connecting R¹ and Y is in the range of 8-14; and (3) when V is -(phenyl)-Q--, then either: U is not a direct bond (i.e., U is not --(CH₂)_(n) -- where n=0) or Q is not a direct bond (i.e., Q is not --(CH₂)_(n) -- where n=0).
 4. A compound of claim 2 of Formula IIIa, IIIb or IIIc: ##STR49## including enantiomeric or diasteriomeric forms thereof, or mixtures of enantiomeric or diasteriomeric forms thereof, or pharmaceutically acceptable salt thereof wherein:R¹ --U taken together are selected from: ##STR50## R² and R³ are independently selected from: H, C₁ -C₄ alkoxy, halogen, C₁ -C₆ alkyl, or C₃ -C₆ alkenyl; V is selected from:--(CH₂)_(n) --, --(C₁ -C₆ alkylene)-Q--, substituted with 0-1 groups independently selected from R¹³ or, --(C₂ -C₇ alkenylene)-Q--, substituted with 0-1 groups independently selected from R¹³, or -(phenyl)-Q--, said phenyl substituted with 0-1 groups independently selected from R¹³, Q is selected from:--(CH₂)_(n) --, --O--, --N(R¹²)--, --N(R¹⁰)C(═O)--, or --C(═O)N(R¹⁰)--; R⁷ is selected from:H, hydroxy, C₁ -C₄ alkoxy, C₁ -C₄ alkylcarbonyl, --N(R¹⁰)(R¹¹), CO₂ R^(18a), SO₂ N(R¹⁰)R¹¹, or OR¹⁰ ; R⁸ is selected from:H, CONR¹⁷ R^(18a), C₁ -C₁₀ alkyl, C₂ -C₁₀ alkenyl, C₂ -C₁₀ alkynyl, C₃ -C₈ cycloalkyl, pyridinyl, or aryl, wherein said aryl or pyridinyl groups are optionally substituted with 0-3 substituents selected from the group consisting of: C₁ -C₄ alkyl, C₁ -C₄ alkoxy, aryl, halo, cyano, CF₃, and NO₂ R⁹ is selected from: H or --NHR¹⁶ ; R¹⁰ is selected from H or C₁ -C₁₀ alkyl; R¹¹ is selected from hydrogen, hydroxy, C₁ to C₈ alkyl, C₃ -C₆ alkenyl, C₃ to C₁₁ cycloalkyl, C₄ to C₁₁ cycloalkylmethyl, C₁ -C₆ alkoxy, benzyloxy, C₆ to C₁₀ aryl, heteroaryl, heteroarylalkyl, C₇ to C₁₁ arylalkyl, or adamantylmethyl; R¹³ is selected from: H, hydroxy, C₁ -C₁₀ alkoxy, N(R¹⁰)R¹¹, --N(R¹⁶)R¹⁷, C₁ -C₁₀ alkyl substituted with 0-2 R⁷, aryl substituted with 0-3 R⁷, heteroaryl substituted with 0-2 R⁷, or C₁ -C₆ alkylcarbonyl; R¹⁶ is selected from:--C(═O)--O--R^(18a), --SO₂ --R^(18a) or, --SO₂ --NHR^(18a) ; R^(18a) is selected from: C₁ -C₈ alkyl, C₃ -C₁₁ cycloalkyl, aryl(C₁ -C₆ alkyl)-, (C₁ -C₆ alkyl)aryl, heteroaryl(C₁ -C₆ alkyl)-, (C₁ -C₆ alkyl)heteroaryl, biaryl(C₁ -C₆ alkyl), heteroaryl, or aryl, wherein said aryl or heteroaryl groups are optionally substituted with 0-2 R¹⁹ ; R¹⁹ is selected from: H, Br, F, Cl, CF₃, CN, NO₂, NHR¹¹, C₁ -C₄ alkyl, aryl, aryl(C₁ -C₄ alkyl)-, C₁ -C₄ alkoxy, C₁ -C₄ alkoxycarbonyl, or --O-aryl, wherein said aryl groups are optionally substituted with 0-3 substituents selected from a group consisting of halogen, CF₃, C₁ -C₃ alkyl, or C₁ -C₃ alkoxy; R²⁰ is selected from:hydroxy; C₁ to C₁₀ alkoxy; methylcarbonyloxymethoxy-; ethylcarbonyloxymethoxy-; t-butylcarbonyloxymethoxy-; cyclohexylcarbonyloxymethoxy-; 1-(methylcarbonyloxy)ethoxy-; 1-(ethylcarbonyloxy)ethoxy-; 1-(t-butylcarbonyloxy)ethoxy-; 1-(cyclohexylcarbonyloxy)ethoxy-; i-propyloxycarbonyloxymethoxy-; t-butyloxycarbonyloxymethoxy-; 1-(i-propyloxycarbonyloxy)ethoxy-; 1-(cyclohexyloxycarbonyloxy)ethoxy-; 1-(t-butyloxycarbonyloxy)ethoxy-; dimethylaminoethoxy-; diethylaminoethoxy-; (5-methyl-1,3-dioxacyclopenten-2-on-4-yl)methoxy-; (5-(t-butyl)-1,3-dioxacyclopenten-2-on-4-yl)methoxy-; (1,3-dioxa-5-phenyl-cyclopenten-2-on-4-yl)methoxy- or; 1-(2-(2-methoxypropyl)carbonyloxy)ethoxy-; n is 0-4; q is 0-1; with the proviso that n, and q are chosen such that the number of atoms connecting R¹ and COR²⁰ is in the range of 8-14.
 5. A compound of claim 1, and enantiomeric or diasteriomeric forms thereof, or mixtures of enantiomeric or diastereomeric forms thereof, or pharmaceutically acceptable salt forms thereof selected from the group consisting of:3- 3- 3-(imidazolin-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid, 3- 3- 3-(imidazolin-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(n-butyloxycarbonyl-amino)propionic acid, 3- 3- 3-(imidazolin-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 3-(imidazolin-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(n-butylsulfonylamino)-propionic acid, 3- 3- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid, 3- 3- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonyl amino!-2-(n-butyloxycarbonylamino)propionic acid, 3- 3- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(n-butylsulfonyl)aminopropionic acid, 3- 3- 4-(imidazolin-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid, 3- 3- 4-(imidazolin-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(n-butyloxycarbonyl-amino)propionic acid, 3- 3- 4-(imidazolin-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 4-(imidazolin-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(n-butylsulfonylamino)propionic acid, 3- 3- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid, 3- 3- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-5-ylcarbonyl amino!-2-(n-butyloxycarbonylamino)propionic acid, 3- 3- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(n-butylsulfonyl)aminopropionic acid, 3- 3- 3-(imidazolin-2-ylamino)propyl!isoxazolin-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid, 3- 3- 3-(imidazolin-2-ylamino)propyl!isoxazolin-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid, 3- 3- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 3-(2-aminothiazol-4-yl)propyl!isoxazolin-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 3-(2-aminothiazol-4-yl)propyl!isoxazolin-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid, 3- 3- 4-(imidazolin-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6-trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6-trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 4-(imidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid, 3- 3- 4-(imidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(phenylsulfonylamino)-propionic acid, 3- 3- 4-(imidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((2,6,dichlorophenyl)sulfonylamino)propionic acid, 3- 3- 4-(imidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 4-(imidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((4-biphenyl)sulfonyl-amino)propionic acid, 3- 3- 4-(imidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid, 3- 3- 3-(imidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-benzyloxycarbonylamino)propionic acid, 3- 3- 3-(imidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 3-(imidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-((2,6,dichlorophenyl)sulfonylamino)propionic acid, 3- 3- 3-(imidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 3-(imidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-((4-biphenyl)sulfonylamino)propionic acid, 3- 3- 3-(imidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid, 3- 3- 2-(imidazol-2-ylamino)ethyl!isoxazolin-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid, 3- 3- 2-(imidazol-2-ylamino)ethyl!isoxazolin-5-ylcarbonylamino!-2-(phenylsulfonylamino)-propionic acid, 3- 3- 2-(imidazol-2-ylamino)ethyl!isoxazolin-5-ylcarbonylamino!-2-((2,6,dichlorophenyl)sulfonylamino)propionic acid, 3- 3- 2-(imidazol-2-ylamino)ethyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 2-(imidazol-2-ylamino)ethyl!isoxazolin-5-ylcarbonylamino!-2-((4-biphenyl)sulfonyl-amino)propionic acid, 3- 3- 2-(imidazol-2-ylamino)ethyl!isoxazolin-5-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid, 3- 3- 3-(imidazol-2-ylaminocarbonyl)propyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 3-(2-aminoimidazol-4-yl)propyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 2-(2-aminoimidazol-4-yl)ethyl!isoxazolin-5-ylmethylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 4-(benzimidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 3-(benzimidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 3-(benzimidazol-2-ylaminocarbonyl)propyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 4-(4-methylimidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 3-(4-methylimidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 4-(4,5-dimethylimidazol-2-ylamino)butyl!-isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 3-(4,5-dimethylimidazol-2-ylamino)propyl!-isoxazolin-5-ylmethylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 3-(4,5-dimethylimidazol-2-ylaminocarbonyl)propyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 4-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 3-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 4-(pyridin-2-ylamino)butyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 3-(pyridin-2-ylamino)propyl!isoxazolin-5-ylmethylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 3-(2-pyridin-6-yl)propyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 2-(2-aminopyridin-6-yl)ethyl!isoxazolin-5-ylmethylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 3- 3-(7-azabenzimidazol-2-yl)propyl!isoxazolin-5-ylcarbonylamino!-2-((2,4,6,trimethylphenyl)sulfonylamino)propionic acid, 3- 5- 3-(imidazolin-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid, 3- 5- 3-(imidazolin-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(n-butyloxycarbonyl-amino)propionic acid, 3- 5- 3-(imidazolin-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 5- 3-(imidazolin-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid, 3- 5- 3-(imidazolin-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(n-butylsulfonylamino)-propionic acid, 3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid, 3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonyl amino!-2-(n-butyloxycarbonylamino)propionic acid, 3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid, 3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(n-butylsulfonyl)aminopropionic acid, 3- 5- 4-(imidazolin-2-yl amino)butyl!isoxazolin-3-ylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid, 3- 5- 4-(imidazolin-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(n-butyloxycarbonylamino)propionic acid, 3- 5- 4-(imidazolin-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 5- 4-(imidazolin-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(n-butylsulfonylamino)propionic acid, 3- 5- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid, 3- 5- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-3-ylcarbonyl amino!-2-(n-butyloxycarbonylamino)propionic acid, 3- 5- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 5- 4-(tetrahydropyrimid-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(n-butylsulfonyl)aminopropionic acid, 3- 5- 3-(imidazol-2-yl amino)propyl!isoxazolin-3-ylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid, 3- 5- 3-(imidazolin-2-ylamino)propyl!isoxazolin-3-ylcarbonylamino!-2-(n-propyloxycarbonylamino)propionic acid, 3- 5- 3-(imidazolin-2-ylamino)propyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 5- 3-(imidazolin-2-ylamino)propyl!isoxazolin-3-ylcarbonylamino!-2-(n-propylsulfonylamino)propionic acid, 3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid, 3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylmethylcarbonylamino!-2-(n-propyloxycarbonylamino)propionic acid, 3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 5- 3-(tetrahydropyrimid-2-ylamino)propyl!isoxazolin-3-ylcarbonylamino!-2-(n-propylsulfonyl)aminopropionic acid, 3- 5- 2-(imidazolin-2-ylamino)ethyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 5- 4-(pyridin-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 5- 4-(pyridin-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,6-dichlorophenylsulfonylamino)propionic acid, 3- 5- 4-(pyridin-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenyl-sulfonylamino)propionic acid, 3- 5- 4-(pyridin-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(4-biphenylsulfonylamino)propionic acid, 3- 5- 4-(pyridin-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid, 3- 5- 3-(2-aminopyridin-6-yl)propyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenyl sulfonylamino)propionic acid, 3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)-propionic acid, 3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,6-dichlorophenylsulfonylamino)propionic acid, 3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenyl-sulfonylamino)propionic acid, 3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(4-biphenylsulfonylamino)propionic acid, 3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid, 3- 5- 3-(2-aminoimidazol-4-yl)propyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)-propionic acid, 3- 5- 3-(2-aminoimidazol-4-yl)propyl!isoxazolin-3-ylcarbonylamino!-2-(2,6-dichlorophenylsulfonylamino)propionic acid, 3- 5- 3-(2-aminoimidazol-4-yl)propyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenyl sulfonylamino)propionic acid, 3- 5- 3-(2-aminoimidazol-4-yl)propyl!isoxazolin-3-ylcarbonylamino!-2-(4-biphenylsulfonylamino)propionic acid, 3- 5- 3-(2-aminoimidazol-4-yl)propyl!isoxazolin-3-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid, 3- 5- 2-(imidazol-2-ylamino)ethyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)-propionic acid, 3- 5- 2-(imidazol-2-ylamino)ethyl!isoxazolin-3-ylcarbonylamino!-2-(2,6-dichlorophenylsulfonylamino)propionic acid, 3- 5- 2-(imidazol-2-ylamino)ethyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenyl-sulfonylamino)propionic acid, 3- 5- 2-(imidazol-2-ylamino)ethyl!isoxazolin-3-ylcarbonylamino!-2-(4-biphenylsulfonylamino)propionic acid, 3- 5- 2-(imidazol-2-ylamino)ethyl!isoxazolin-3-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid, 3- 5- 3-(imidazol-2-ylaminocarbonyl)propyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid, 3- 5- 3-(benzimidazol-2-ylaminocarbonyl)propyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid, 3- 5- 4-(benzimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 5- 4-(benzimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,6-dichlorophenylsulfonylamino)propionic acid, 3- 5- 4-(benzimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid, 3- 5- 4-(benzimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(4-biphenylsulfonylamino)propionic acid, 3- 5- 4-(benzimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid, 3- 5- 4-(4-methylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 5- 4-(4-methylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,6-dichlorophenylsulfonylamino)propionic acid, 3- 5- 4-(4-methylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid, 3- 5- 4-(4-methylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(4-biphenylsulfonylamino)propionic acid, 3- 5- 4-(4-methylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid, 3- 5- 4-(4,5-dimethylimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 5- 4-(4,5-dimethylimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(2,6-dichlorophenylsulfonylamino)propionic acid, 3- 5- 4-(4,5-dimethylimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid, 3- 5- 4-(4,5-dimethylimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(4-biphenylsulfonylamino)propionic acid, 3- 5- 4-(4,5-dimethylimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid, 3- 5- 4-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 5- 4-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(2,6-dichlorophenylsulfonylamino)propionic acid, 3- 5- 4-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid, 3- 5- 4-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(4-biphenylsulfonylamino)propionic acid, 3- 5- 4-(4-,5,6,7-tetrahydrobenzimidazol-2-ylamino)butyl!-isoxazolin-3-ylcarbonylamino!-2-(1-naphthylsulfonylamino)propionic acid, 3- 5- 3-(7-azabenzimidazol-2-yl)propyl!isoxazolin-3-ylcarbonylamino!-2-(2,4,6-trimethylphenylsulfonylamino)propionic acid, 3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2- (2,6-dimethyl-4-phenyl)phenylsulfonylamino!propionic acid, 3- 5- 4-(4-methylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,6-dimethyl-4-phenyl)phenylsulfonylamino!propionic acid, 3- 5- 4-(4,5-dimethylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2- (2,6-dimethyl-4-phenyl)phenylsulfonylamino!propionic acid, 3- 5- 4-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2- (2,6-dimethyl-4-phenyl)phenylsulfonylamino!propionic acid, 3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2- (2,6-dichloro-4-phenyl)phenylsulfonylamino!propionic acid, 3- 5- 4-(4-methylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2-(2,6-dichloro-4-phenyl)phenylsulfonylamino!propionic acid, 3- 5- 4-(4,5-dimethylimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2- (2,6-dichloro-4-phenyl)phenylsulfonylamino!propionic acid, 3- 5- 4-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-2- (2,6-dichloro-4-phenyl)phenylsulfonylamino!propionic acid, 3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-3-(phenylsulfonylmethyl)propionic acid, 3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-3-(1-adamantylmethylaminocarbonyl)propionic acid, 3- 5- 4-(imidazol-2-ylamino)butyl!isoxazolin-3-ylcarbonylamino!-3-(3-pyridinyl)propionic acid, 3- 3- 3-(imidazolin-2-ylamino)propyloxy!isoxazol-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)-propionic acid, 3- 3- 3-(imidazolin-2-ylamino)propyloxy!isoxazol-5-yl carbonyl amino!-2-(n-butyloxycarbonyl-amino)propionic acid, 3- 3- 3-(imidazolin-2-ylamino)propyloxy!isoxazol-5-yl carbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 3-(imidazolin-2-ylamino)propyloxy!isoxazol-5-yl carbonyl amino!-2-(n-butylsulfonylamino)-propionic acid, 3- 3- 3-(tetrahydropyrimid-2-ylamino)propyloxy!-isoxazol-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid, 3- 3- 3-(tetrahydropyrimid-2-ylamino)propyloxy!-isoxazol-5-ylcarbonyl amino!-2-(n-butyloxycarbonylamino)propionic acid, 3- 3- 3-(tetrahydropyrimid-2-ylamino)propyloxy!-isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 3-(tetrahydropyrimid-2-ylamino)propyloxy!-isoxazol-5-yl carbonylamino!-2-(n-butylsulfonyl)aminopropionic acid, 3- 3- 2-(imidazolin-2-yl amino)ethyloxy!isoxazol-5-yl carbonylamino!-2-(benzyloxycarbonylamino)-propionic acid, 3- 3- 3-(imidazolin-2-ylamino)ethyloxy!isoxazol-5-yl carbonylamino!-2-(n-butyloxycarbonylamino)propionic acid, 3- 3- 3-(imidazolin-2-ylamino)ethyloxy!isoxazol-5-yl carbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 3-(imidazolin-2-ylamino)ethyloxy!isoxazol-5-ylcarbonylamino!-2-(n-butylsulfonylamino)propionic acid, 3- 3- 3-(tetrahydropyrimid-2-yl amino)ethyloxy!-isoxazol-5-ylcarbonylamino!-2-(benzyloxycarbonylamino)propionic acid, 3- 3- 3-(tetrahydropyrimid-2-ylamino)ethyloxy!-isoxazol-5-ylcarbonylamino!-2-(n-butyloxycarbonylamino)propionic acid, 3- 3- 3-(tetrahydropyrimid-2-ylamino)ethyloxy!-isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 3-(tetrahydropyrimid-2-ylamino)ethyloxy!-isoxazol-5-ylcarbonylamino!-2-(n-butylsulfonylamino)propionic acid, 3- 3- 3-(imidazol-2-ylamino)propyloxy!isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 3-(benzimidazol-2-ylamino)propyloxy!isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 3-(4-methylimidazol-2-ylamino)propyloxy!-isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 3-(4,5-dimethylimidazol-2-ylamino)propyloxy!-isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 3-(4,5,6,7-tetrahydrobenzimidazol-2-ylamino)propyloxy!-isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 3-(pyridin-2-ylamino)propyloxy!isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, 3- 3- 3-(imidazol-2-ylaminocarbonyl)ethoxy!isoxazol-5-ylcarbonylamino!-2-(phenylsulfonylamino)propionic acid, and prodrug ester forms thereof, wherein the hydrogen of the hydroxy group of the propionic acid moiety is substituted with a group selected from:C₁ -C₁₀ alkyl; methylcarbonyloxymethyl-; ethylcarbonyloxymethyl-; t-butylcarbonyloxymethyl-; cyclohexylcarbonyloxymethyl-; 1-(methylcarbonyloxy)ethyl-; 1-(ethylcarbonyloxy)ethyl-; 1(t-butylcarbonyloxy)ethyl-; 1-(cyclohexylcarbonyloxy)ethyl-; i-propyloxycarbonyloxymethyl-; t-butyloxycarbonyloxymethyl-; 1-(i-propyloxycarbonyloxy)ethyl-; 1-(cyclohexyloxycarbonyloxy)ethyl-; 1-(t-butyloxycarbonyloxy)ethyl-; dimethylaminoethyl-; diethylaminoethyl-: (5-methyl-1,3-dioxacyclopenten-2-on-4-yl)methyl-; (5-(t-butyl)-1,3-dioxacyclopenten-2-on-4-yl)methyl-; (1,3-dioxa-5-phenyl-cyclopenten-2-on-4-yl)methyl-; or 1-(2-(2-methoxypropyl)carbonyloxy)ethyl-.
 6. A method of treating angiogenic disorders, inflammation, bone degradation, or thrombosis, comprising administering to a host in need of such treatment a therapeutically effective amount of a compound of claim
 1. 7. A method of treating angiogenic disorders, inflammation, bone degradation, or thrombosis, comprising administering to a host in need of such treatment a therapeutically effective amount of a compound of claim
 2. 8. A method of treating angiogenic disorders, inflammation, bone degradation, or thrombosis, comprising administering to a host in need of such treatment a therapeutically effective amount of a compound of claim
 3. 9. A method of treating angiogenic disorders, inflammation, bone degradation, or thrombosis, comprising administering to a host in need of such treatment a therapeutically effective amount of a compound of claim
 4. 10. A method of treating angiogenic disorders, inflammation, bone degradation, or thrombosis, comprising administering to a host in need of such treatment a therapeutically effective amount of a compound of claim
 5. 11. A pharmaceutical composition comprising a therapeutically effective amount of a compound of claim 1 and a pharmaceutically acceptable carrier.
 12. A pharmaceutical composition comprising a therapeutically effective amount of a compound of claim 2 and a pharmaceutically acceptable carrier.
 13. A pharmaceutical composition comprising a therapeutically effective amount of a compound of claim 3 and a pharmaceutically acceptable carrier.
 14. A pharmaceutical composition comprising a therapeutically effective amount of a compound of claim 4 and a pharmaceutically acceptable carrier.
 15. A pharmaceutical composition comprising a therapeutically effective amount of a compound of claim 5 and a pharmaceutically acceptable carrier.
 16. A method for the treatment of thrombosis which comprises administering to a host in need of such treatment a therapeutically effective amount of a compound of claim 1 in combination with one or more additional therapeutic agents selected from: a thrombolytic agent, an anti-coagulant agent, or an anti-platelet agent.
 17. A method of inhibiting angiogenesis, comprising administering to a host in need of such inhibition a therapeutically effective amount of a compound of claim
 1. 18. A method of inhibiting angiogenesis, comprising administering to a host in need of such inhibition a therapeutically effective amount of a compound of claim
 2. 19. A method of inhibiting angiogenesis, comprising administering to a host in need of such inhibition a therapeutically effective amount of a compound of claim
 3. 20. A method of inhibiting angiogenesis, comprising administering to a host in need of such inhibition a therapeutically effective amount of a compound of claim
 4. 21. A method of inhibiting angiogenesis, comprising administering to a host in need of such inhibition a therapeutically effective amount of a compound of claim
 5. 